Legend
| MIN | MiniPanel™ |
| MAX | MaxPanel™ |
| COM | ComprehensivePanel™ |
| + | PanelPlus® |
For genes that require ancillary assays beyond NGS, we offer our PanelPlus® tests. All tests can expand to Whole Exome Sequencing, with new samples needed only for MiniPanel™ and MaxPanel™ testing tiers.
| Choose column to Search |
| Legend | Disease Name | Gene | Category | TestCode | |
|---|---|---|---|---|---|
| MAX | Arrhythmia Panel, Comprehensive | 73 genes | Cardiology | D4105 | |
| MAX | Arrhythmia Panel, STAT Comprehensive | 73 genes | Cardiology | D4105F | |
| MAX | Arrhythmogenic Cardiomyopathy Panel | 24 genes | Cardiology | D4100 | |
| MAX | Arrhythmogenic Cardiomyopathy Panel, STAT | 24 genes | Cardiology | D4100F | |
| MIN | Brugada Syndrome Panel | 8 genes | Cardiology | D4108 | |
| MIN | Brugada Syndrome Panel, STAT | 8 genes | Cardiology | D4108F | |
| COM | Cardiomyopathy Panel, Comprehensive | 122 genes | Cardiology | D4101 | |
| COM | Cardiomyopathy Panel, STAT Comprehensive | 122 genes | Cardiology | D4101F | |
| COM | Cardiomyopathy and Skeletal Muscle Disease Panel | 158 genes | Cardiology | D4109 | |
| COM | Cardiomyopathy and Skeletal Muscle Disease Panel, STAT | 158 genes | Cardiology | D4109F | |
| MIN | Catecholaminergic Polymorphic Ventricular Tachycardia Panel | 10 genes | Cardiology | D5201 | |
| MAX | Dilated Cardiomyopathy Panel | 48 genes | Cardiology | D4102 | |
| MAX | Dilated Cardiomyopathy Panel, STAT | 48 genes | Cardiology | D4102F | |
| MAX | Hypertrophic Cardiomyopathy Panel | 39 genes | Cardiology | D4103 | |
| MAX | Hypertrophic Cardiomyopathy Panel, STAT | 39 genes | Cardiology | D4103F | |
| MAX | Long QT Syndrome Panel | 17 genes | Cardiology | D4106 | |
| MAX | Long QT Syndrome Panel, STAT | 17 genes | Cardiology | D4106F | |
| MAX | Marfan/TAAD Panel | 25 genes | Cardiology | D4110 | |
| MAX | Marfan/TAAD Panel, STAT | 25 genes | Cardiology | D4110F | |
| MIN | Pulmonary Arterial Hypertension Panel | 8 genes | Cardiology | D5226 | |
| MAX | Deafness Non-Syndromic Sensorineural Autosomal Recessive Panel | 46 genes | Hearing loss | D4401 | |
| MAX | Deafness Non-Syndromic Sensorineural Autosomal Recessive Panel, STAT | 46 genes | Hearing loss | D4401F | |
| COM | Hearing Loss Panel, Comprehensive | 146 genes | Hearing loss | D5205 | |
| MAX | Non-Syndromic Sensorineural Deafness Panel | 60 genes | Hearing loss | D5223 | |
| MIN | Treacher Collins Syndrome Sequencing Panel | 3 genes | Hearing loss | D4405 | |
| MIN | Treacher Collins Syndrome Sequencing Panel, STAT | 3 genes | Hearing loss | D4405F | |
| MIN | Usher Syndrome Panel | 14 genes | Hearing loss | D4308 | |
| MIN | Usher Syndrome Panel, STAT | 14 genes | Hearing loss | D4308F | |
| MIN | Waardenburg Syndrome Panel | 7 genes | Hearing loss | D4402 | |
| MIN | Waardenburg Syndrome Panel, STAT | 7 genes | Hearing loss | D4402F | |
| MAX | Breast and Gynecological Cancers Panel | 26 genes | Hereditary Cancer | D4210 | |
| MAX | Breast and Gynecological Cancers Panel, STAT | 26 genes | Hereditary Cancer | D4210F | |
| MAX | Cancer Panel, Comprehensive | 82 genes | Hereditary Cancer | D4205 | |
| MAX | Cancer Panel, STAT Comprehensive | 82 genes | Hereditary Cancer | D4205F | |
| MAX | Colorectal Cancer Panel | 19 genes | Hereditary Cancer | D4200 | |
| MAX | Colorectal Cancer Panel | 19 genes | Hereditary Cancer | D4200F | |
| MIN | Hereditary Breast and Ovarian Cancer Syndrome Panel | 2 genes | Hereditary Cancer | D4209 | |
| MIN | Hereditary Breast and Ovarian Cancer Syndrome Panel, STAT | 2 genes | Hereditary Cancer | D4209F | |
| MIN | Lynch Syndrome Panel | 5 genes | Hereditary Cancer | D5219 | |
| MIN | Multiple Endocrine Neoplasias/Paraganglioma/Pheochromocytoma Panel | 10 genes | Hereditary Cancer | D4203 | |
| MIN | Multiple Endocrine Neoplasias/Paraganglioma/Pheochromocytoma Panel, STAT | 10 genes | Hereditary Cancer | D4203F | |
| MAX | Pancreatic Cancer Panel | 20 genes | Hereditary Cancer | D4201 | |
| MAX | Pancreatic Cancer Panel, STAT | 20 genes | Hereditary Cancer | D4201F | |
| MAX | Pediatric Tumor Panel | 23 genes | Hereditary Cancer | D4207 | |
| MAX | Pediatric Tumor Panel, STAT | 23 genes | Hereditary Cancer | D4207F | |
| MAX | Renal Cancer Panel | 25 genes | Hereditary Cancer | D4204 | |
| MAX | Renal Cancer Panel, STAT | 25 genes | Hereditary Cancer | D4204F | |
| MIN | Tuberous Sclerosis Panel | 2 genes | Hereditary Cancer | D4211 | |
| MIN | Tuberous Sclerosis Panel, STAT | 2 genes | Hereditary Cancer | D4211F | |
| + | Adrenoleukodystrophy Panel with ABCD1 | 15 genes | Metabolic and Mitochondrial | D4043 | |
| MIN | Chronic Pancreatitis Panel | 6 genes | Metabolic and Mitochondrial | D5202 | |
| + | Congenital Adrenal Hyperplasia Panel with CYP21A2 | 7 genes | Metabolic and Mitochondrial | D4584 | |
| + | Congenital Adrenal Hyperplasia Panel with CYP21A2, STAT | 7 genes | Metabolic and Mitochondrial | D4584F | |
| MAX | Congenital Disorders of Glycosylation Panel | 93 genes | Metabolic and Mitochondrial | D4571 | |
| MAX | Congenital Disorders of Glycosylation Panel, STAT | 93 genes | Metabolic and Mitochondrial | D4571F | |
| MIN | Congenital Hypothyroidism | 8 genes | Metabolic and Mitochondrial | D4574 | |
| MIN | Congenital Hypothyroidism, STAT | 8 genes | Metabolic and Mitochondrial | D4574F | |
| + | Creatine Deficiency Syndrome Panel | 3 genes | Metabolic and Mitochondrial | D5209 | |
| MIN | Elevated C4 Panel | 3 genes | Metabolic and Mitochondrial | D4537 | |
| MIN | Elevated C4 Panel, STAT | 3 genes | Metabolic and Mitochondrial | D4537F | |
| MIN | Elevated C5-OH Panel | 11 genes | Metabolic and Mitochondrial | D4541 | |
| MIN | Elevated C5-OH Panel, STAT | 11 genes | Metabolic and Mitochondrial | D4541F | |
| MIN | Elevated Phenylalanine Panel | 5 genes | Metabolic and Mitochondrial | D4549 | |
| MIN | Elevated Phenylalanine Panel, STAT | 5 genes | Metabolic and Mitochondrial | D4549F | |
| MAX | Fatty Acid Oxidation Defects Panel | 16 genes | Metabolic and Mitochondrial | D4572 | |
| MAX | Fatty Acid Oxidation Defects Panel, STAT | 16 genes | Metabolic and Mitochondrial | D4572F | |
| MIN | Galactosemia Panel | 3 genes | Metabolic and Mitochondrial | D4563 | |
| MIN | Galactosemia Panel, STAT | 3 genes | Metabolic and Mitochondrial | D4563F | |
| MAX | Glycogen Storage Disease Panel, Comprehensive | 23 genes | Metabolic and Mitochondrial | D4566 | |
| MAX | Glycogen Storage Disease Panel, STAT Comprehensive | 23 genes | Metabolic and Mitochondrial | D4566F | |
| MAX | Hyperammonemia Panel | 48 genes | Metabolic and Mitochondrial | D5215 | |
| MIN | Hyperparathyroidism Panel | 8 genes | Metabolic and Mitochondrial | D5216 | |
| MIN | Hereditary Hemochromatosis Panel | 5 genes | Metabolic and Mitochondrial | D4700 | |
| MIN | Hereditary Hemochromatosis Panel, STAT | 5 genes | Metabolic and Mitochondrial | D4700F | |
| MIN | Krabbe Disease Panel | 2 genes | Metabolic and Mitochondrial | D4506 | |
| MIN | Krabbe Disease Panel, STAT | 2 genes | Metabolic and Mitochondrial | D4506F | |
| + | Lysosomal Storage Disorder Panel with GBA and IDS | 12 genes | Metabolic and Mitochondrial | D3001 | |
| + | Lysosomal Storage Disorders Panel with GBA and IDS, Comprehensive | 51 genes | Metabolic and Mitochondrial | D4501 | |
| + | Lysosomal Storage Disorders Panel with GBA and IDS, STAT Comprehensive | 51 genes | Metabolic and Mitochondrial | D4501F | |
| MIN | Maple Syrup Urine Disease Panel | 5 genes | Metabolic and Mitochondrial | D4561 | |
| MIN | Maple Syrup Urine Disease Panel, STAT | 5 genes | Metabolic and Mitochondrial | D4561F | |
| MIN | Metachromatic Leukodystrophy Panel | 7 genes | Metabolic and Mitochondrial | D4508 | |
| MIN | Metachromatic Leukodystrophy Panel, STAT | 7 genes | Metabolic and Mitochondrial | D4508F | |
| MAX | Methylmalonic Acidemia Panel | 17 genes | Metabolic and Mitochondrial | D4589 | |
| MAX | Methylmalonic Acidemia Panel, STAT | 17 genes | Metabolic and Mitochondrial | D4589F | |
| COM | Mitochondrial Encephalopathy/Leigh Syndrome Nuclear Gene Panel | 146 genes | Metabolic and Mitochondrial | D4607 | |
| COM | Mitochondrial Encephalopathy/Leigh Syndrome Nuclear Gene Panel, STAT | 146 genes | Metabolic and Mitochondrial | D4607F | |
| COM | Mitochondrial Nuclear Gene Panel, Comprehensive | 254 genes | Metabolic and Mitochondrial | D4606 | |
| COM | Mitochondrial Nuclear Gene Panel, STAT Comprehensive | 254 genes | Metabolic and Mitochondrial | D4606F | |
| + | Mucopolysaccharidoses (MPS) Panel, Comprehensive | 23 genes | Metabolic and Mitochondrial | D4502 | |
| + | Mucopolysaccharidoses (MPS) Panel, STAT Comprehensive | 23 genes | Metabolic and Mitochondrial | D4502F | |
| MAX | Nephrotic Syndrome Panel | 30 genes | Metabolic and Mitochondrial | D4613 | |
| MAX | Nephrotic Syndrome Panel, STAT | 30 genes | Metabolic and Mitochondrial | D4613F | |
| MIN | Primary Hyperoxaluria Panel | 3 genes | Metabolic and Mitochondrial | D5225 | |
| MIN | Tyrosinemia Panel | 3 genes | Metabolic and Mitochondrial | D4562 | |
| MIN | Tyrosinemia Panel, STAT | 3 genes | Metabolic and Mitochondrial | D4562F | |
| MIN | Urea Cycle Disorders Panel | 15 genes | Metabolic and Mitochondrial | D4532 | |
| MIN | Urea Cycle Disorders Panel, STAT | 15 genes | Metabolic and Mitochondrial | D4532F | |
| + | Adrenoleukodystrophy Panel with ABCD1 | 15 genes | Neurology | D4043 | |
| MIN | Aicardi-Goutieres Syndrome Panel | 7 genes | Neurology | D4014 | |
| MIN | Aicardi-Goutieres Syndrome Panel, STAT | 7 genes | Neurology | D4014F | |
| MIN | Brain Iron Accumulation Syndromes Panel | 9 genes | Neurology | D4016 | |
| MIN | Brain Iron Accumulation Syndromes Panel, STAT | 9 genes | Neurology | D4016F | |
| MAX | Brain Malformations Panel, Comprehensive | 93 genes | Neurology | D4023 | |
| MAX | Brain Malformations Panel, STAT Comprehensive | 93 genes | Neurology | D4023F | |
| MIN | Ceroid Lipofuscinosis Panel | 13 genes | Neurology | D4026 | |
| MIN | Ceroid Lipofuscinosis Panel, STAT | 13 genes | Neurology | D4026F | |
| MAX | Charcot Marie Tooth Disease Panel | 62 genes | Neurology | D4037 | |
| MAX | Charcot Marie Tooth Disease Panel, STAT | 62 genes | Neurology | D4037F | |
| MAX | Dystonia Panel | 17 genes | Neurology | D4012 | |
| MAX | Dystonia Panel, STAT | 17 genes | Neurology | D4012F | |
| COM | Epilepsy Panel, Comprehensive | 99 genes | Neurology | D4002 | |
| COM | Epilepsy Panel, STAT Comprehensive | 99 genes | Neurology | D4002F | |
| + | Expanded Leukodystrophy Panel with ABCD1 | 291 genes | Neurology | D5211 | |
| COM | Focused Autism and Intellectual Disability Panel | 263 genes | Neurology | D5130 | |
| COM | Focused Autism and Intellectual Disability Panel, STAT | 263 genes | Neurology | D5130F | |
| MIN | Hemiplegic Migraine Panel | 4 genes | Neurology | D5213 | |
| MAX | Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel | 33 genes | Neurology | D4019 | |
| MAX | Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel, STAT | 33 genes | Neurology | D4019F | |
| COM | Hereditary Neuropathy Sequencing Panel | 122 genes | Neurology | D4022 | |
| COM | Hereditary Neuropathy Sequencing Panel, STAT | 122 genes | Neurology | D4022F | |
| MAX | Infantile Epilepsy Panel | 76 genes | Neurology | D4003 | |
| MAX | Infantile Epilepsy Panel, STAT | 76 genes | Neurology | D4003F | |
| MAX | Joubert and Meckel-Gruber Syndromes Panel | 30 genes | Neurology | D4013 | |
| MAX | Joubert and Meckel-Gruber Syndromes Panel, STAT | 30 genes | Neurology | D4013F | |
| MAX | Lissencephaly Panel | 24 genes | Neurology | D4025 | |
| MAX | Lissencephaly Panel, STAT | 24 genes | Neurology | D4025F | |
| MIN | Myoclonic Dystonia Panel | 2 genes | Neurology | D4010 | |
| MIN | Myoclonic Dystonia Panel, STAT | 2 genes | Neurology | D4010F | |
| MAX | Nervous System and Brain Tumor Panel | 17 genes | Neurology | D5222 | |
| MAX | Neurodegeneration Panel | 38 genes | Neurology | D4021 | |
| MAX | Neurodegeneration Panel, STAT | 38 genes | Neurology | D4021F | |
| MAX | Rett, Angelman and Related Syndromes Panel | 20 genes | Neurology | D5203 | |
| MAX | Spastic Paraplegia Panel Complete | 55 genes | Neurology | D4011 | |
| MAX | Spastic Paraplegia Panel Complete, STAT | 55 genes | Neurology | D4011F | |
| MAX | Charcot Marie Tooth Disease Panel | 62 genes | Neuromuscular | D4037 | |
| MAX | Charcot Marie Tooth Disease Panel, STAT | 62 genes | Neuromuscular | D4037F | |
| MAX | Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel | 33 genes | Neuromuscular | D4019 | |
| MAX | Hereditary Dementia and Amyotrophic Lateral Sclerosis Panel, STAT | 33 genes | Neuromuscular | D4019F | |
| COM | Hereditary Neuropathy Sequencing Panel | 122 genes | Neuromuscular | D4022 | |
| COM | Hereditary Neuropathy Sequencing Panel, STAT | 122 genes | Neuromuscular | D4022F | |
| MAX | Hereditary Parkinson’s Disease and Parkinsonism Panel | 21 genes | Neuromuscular | D4018 | |
| MAX | Hereditary Parkinson’s Disease and Parkinsonism Panel, STAT | 21 genes | Neuromuscular | D4018F | |
| MAX | Muscular Dystrophy Panel, Comprehensive | 56 genes | Neuromuscular | D4032 | |
| MAX | Muscular Dystrophy Panel, STAT Comprehensive | 56 genes | Neuromuscular | D4032F | |
| COM | Neuromuscular Disorders Panel, Comprehensive | 133 genes | Neuromuscular | D4035 | |
| COM | Neuromuscular Disorders Panel, STAT Comprehensive | 133 genes | Neuromuscular | D4035F | |
| MAX | Neuropathies Panel, Comprehensive | 81 genes | Neuromuscular | D4020 | |
| MAX | Neuropathies Panel, STAT Comprehensive | 81 genes | Neuromuscular | D4020F | |
| MAX | Limb-Girdle Muscular Dystrophy Panel | 30 genes | Neuromuscular | D5218 | |
| MIN | Periodic Paralysis Panel | 8 genes | Neuromuscular | D5224 | |
| MAX | Albinism Panel | 28 genes | Ophthalmology | D4309 | |
| MAX | Albinism Panel, STAT | 28 genes | Ophthalmology | D4309F | |
| MAX | Cataract Panel | 69 genes | Ophthalmology | D5200 | |
| MIN | Congenital Stationary Night-Blindness Panel | 12 genes | Ophthalmology | D5207 | |
| COM | Eye Disorders Panel, Comprehensive | 211 genes | Ophthalmology | D4306 | |
| COM | Eye Disorders Panel, Comprehensive STAT | 211 genes | Ophthalmology | D4306F | |
| MAX | Glaucoma Panel | 38 genes | Ophthalmology | D5212 | |
| MAX | Leber Congenital Amaurosis Panel | 19 genes | Ophthalmology | D5217 | |
| MIN | Macular Dystrophy/Degeneration/Stargardt Disease Panel | 15 genes | Ophthalmology | D4305 | |
| MIN | Macular Dystrophy/Degeneration/Stargardt Disease Panel, STAT | 15 genes | Ophthalmology | D4305F | |
| MAX | Microphthalmia/Anophthalmia/Coloboma Spectrum Panel | 49 genes | Ophthalmology | D4300 | |
| MAX | Microphthalmia/Anophthalmia/Coloboma Spectrum Panel, STAT | 49 genes | Ophthalmology | D4300F | |
| MIN | Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Panel | 15 genes | Ophthalmology | D4702 | |
| MIN | Pulmonary Fibrosis and Hermansky-Pudlak Syndrome Panel, STAT | 15 genes | Ophthalmology | D4702F | |
| COM | Retina/Photoreceptor Dystrophy Panel | 121 genes | Ophthalmology | D4304 | |
| COM | Retina/Photoreceptor Dystrophy Panel, STAT | 121 genes | Ophthalmology | D4304F | |
| MAX | Retinitis Pigmentosa Panel | 66 genes | Ophthalmology | D4303 | |
| MAX | Retinitis Pigmentosa Panel, STAT | 66 genes | Ophthalmology | D4303F | |
| MIN | Usher Syndrome Panel | 14 genes | Ophthalmology | D4308 | |
| MIN | Usher Syndrome Panel, STAT | 14 genes | Ophthalmology | D4308F | |
| MIN | Vitreoretinopathy Panel | 4 genes | Ophthalmology | D5228 | |
| COM | Ciliopathies Panel | 101 genes | Other Conditions | D4703 | |
| COM | Ciliopathies Panel, STAT | 101 genes | Other Conditions | D4703F | |
| MIN | Cornelia de Lange Syndrome Panel | 8 genes | Other Conditions | D4707 | |
| MIN | Cornelia de Lange Syndrome Panel, STAT | 8 genes | Other Conditions | D4707F | |
| MIN | Ehlers Danlos Panel | 3 genes | Other Conditions | D5210 | |
| MIN | Familial Mediterranean Fever Panel | 9 genes | Other Conditions | D4730 | |
| MIN | Familial Mediterranean Fever Panel, STAT | 9 genes | Other Conditions | D4730F | |
| MIN | Hereditary Hemochromatosis Panel | 5 genes | Other Conditions | D4700 | |
| MIN | Hereditary Hemochromatosis Panel, STAT | 5 genes | Other Conditions | D4700F | |
| MIN | Hereditary Hemorrhagic Telangiectasia Panel | 5 genes | Other Conditions | D4734 | |
| MIN | Hereditary Hemorrhagic Telangiectasia Panel, STAT | 5 genes | Other Conditions | D4734F | |
| MIN | Hereditary Thrombophilia Panel | 7 genes | Other Conditions | D4701 | |
| MIN | Hereditary Thrombophilia Panel, STAT | 7 genes | Other Conditions | D4701F | |
| MIN | Heterotaxy Panel | 11 genes | Other Conditions | D4705 | |
| MIN | Heterotaxy Panel, STAT | 11 genes | Other Conditions | D4705F | |
| MIN | Holoprosencephaly Panel | 10 genes | Other Conditions | D5214 | |
| MIN | Hyper-IgE Syndromes Panel | 4 genes | Other Conditions | D4712 | |
| MIN | Hyper-IgE Syndromes Panel, STAT | 4 genes | Other Conditions | D4712F | |
| MAX | Joubert and Meckel-Gruber Syndromes Panel | 30 genes | Other Conditions | D4013 | |
| MAX | Joubert and Meckel-Gruber Syndromes Panel, STAT | 30 genes | Other Conditions | D4013F | |
| MAX | Limb Malformation: Sequencing Panel | 40 genes | Other Conditions | D4725 | |
| MAX | Limb Malformation: Sequencing Panel, STAT | 40 genes | Other Conditions | D4725F | |
| MAX | MODY Panel | 17 genes | Other Conditions | D4733 | |
| MAX | MODY Panel, STAT | 17 genes | Other Conditions | D4733F | |
| MIN | Myelodysplastic Syndrome/Leukemia Panel | 14 genes | Other Conditions | D5220 | |
| MAX | Noonan and RASopathies Panel | 17 genes | Other Conditions | D4708 | |
| MAX | Noonan and RASopathies Panel, STAT | 17 genes | Other Conditions | D4708F | |
| MAX | Obesity Panel | 35 genes | Other Conditions | D4731 | |
| MAX | Obesity Panel, STAT | 35 genes | Other Conditions | D4731F | |
| MIN | Periodic Fever Syndromes Panel | 12 genes | Other Conditions | D4729 | |
| MIN | Periodic Fever Syndromes Panel, STAT | 12 genes | Other Conditions | D4729F | |
| + | Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis | 21 genes | Other Conditions | D4718 | |
| + | Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis, STAT | 21 genes | Other Conditions | D4718F | |
| MAX | Pulmonary Disease: Comprehensive Sequencing Panel | 52 genes | Other Conditions | D4732 | |
| MAX | Pulmonary Disease: Comprehensive Sequencing Panel, STAT | 52 genes | Other Conditions | D4732F | |
| MIN | Senior-Loken Syndrome Panel | 9 genes | Other Conditions | D5227 | |
| MAX | Skeletal Dysplasia with Increased Bone Density: Sequencing Panel | 22 genes | Other Conditions | D4724 | |
| MAX | Skeletal Dysplasia with Increased Bone Density: Sequencing Panel, STAT | 22 genes | Other Conditions | D4724F | |
| MIN | Treacher Collins Syndrome Sequencing Panel | 3 genes | Other Conditions | D4405 | |
| MIN | Treacher Collins Syndrome Sequencing Panel, STAT | 3 genes | Other Conditions | D4405F |
Malaysia
