Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Common Hereditary Cancer Screening Panel PreventionGenetics United States | 94 | 55 |
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Centogene US, LLC - The Rare Disease Company United States | 114 | 68 |
|
Centogene US, LLC - The Rare Disease Company United States | 156 | 107 |
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SDHC - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 3 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 114 | 68 |
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Centogene AG - the Rare Disease Company Germany | 156 | 107 |
|
SDHC - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
|
Invitae Multi-Cancer + RNA Panel Invitae United States | 143 | 63 |
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Invitae Common Hereditary Cancers + RNA Panel Invitae United States | 114 | 47 |
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PreventionGenetics United States | 36 | 19 |
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Invitae Nuclear Mitochondrial Disorders Panel Invitae United States | 394 | 319 |
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Invitae 59 Gene Actionable Disorders Panel Invitae United States | 57 | 59 |
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Variant Resolution Test for CustomNext-Cancer® (+RNAinsight®) Ambry Genetics United States | 147 | 18 |
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Variant Resolution Test for RenalNext® (+RNAinsight®) Ambry Genetics United States | 57 | 7 |
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Variant Resolution Test for PGLNext® (+RNAinsight®) Ambry Genetics United States | 26 | 1 |
|
Variant Resolution Test for CancerNext-Expanded® (+RNAinsight®) Ambry Genetics United States | 141 | 18 |
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SDHC - hereditary paraganglioma and pheochromocytoma Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 2 | 1 |
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PreventionGenetics United States | 78 | 64 |
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Ambry Genetics United States | 57 | 20 |
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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.