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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
Common Hereditary Cancer Screening Panel PreventionGenetics, part of Exact Sciences United States | 94 | 55 |
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KIT - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 5 | 1 |
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SNAI2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Centogene AG - the Rare Disease Company Germany | 740 | 728 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
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Centogene AG - the Rare Disease Company Germany | 157 | 151 |
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Invitae Common Hereditary Cancers + RNA Panel Invitae United States | 114 | 47 |
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PreventionGenetics, part of Exact Sciences United States | 36 | 19 |
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Invitae Inborn Errors of Immunity and Cytopenias Panel Invitae United States | 755 | 562 |
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Invitae Hypopigmentation Panel Invitae United States | 83 | 46 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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Piebaldism, 172800, Autosomal dominant; PBT (Piebaldism) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Piebaldism, 172800, Autosomal dominant (Piebaldism) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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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.