Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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Myriad Genetics, Inc. United States | 1 | 1 |
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Invitae Treatable Neurometabolic Disorders Panel Invitae United States | 257 | 191 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 328 | 300 |
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PreventionGenetics, part of Exact Sciences United States | 10 | 9 |
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Invitae Metabolic Newborn Screening Confirmation Panel Invitae United States | 201 | 158 |
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Invitae United States | 466 | 297 |
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Invitae Hereditary Spastic Paraplegia Comprehensive Panel Invitae United States | 98 | 62 |
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Baylor Genetics United States | 842 | 637 |
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ARG1 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 1 | 1 |
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Baylor Genetics United States | 1 | 1 |
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ARG1 Deletion/Duplication Analysis Baylor Genetics United States | 1 | 1 |
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ARG1 Comprehensive - Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 1 | 1 |
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Baylor Genetics United States | 25 | 26 |
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Elevated Arginine/Argininemia via the ARG1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Baylor Genetics United States | 1 | 1 |
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NGS Neurodegenerative disorders Multi-Gene Panel (73 genes) Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC Netherlands | 41 | 60 |
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Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
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Integrated Genetics Westborough LabCorp United States | 330 | 746 |
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Targeted Variant, Fetal Analysis Integrated Genetics Westborough LabCorp United States | 292 | 746 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.