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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
HFE Gene Hemochromatosis classical NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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Invitae Expanded Renal Disease Panel Invitae United States | 693 | 388 |
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Centogene AG - the Rare Disease Company Germany | 218 | 135 |
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Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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TSC1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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TSC2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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MTOR - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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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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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
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Invitae Neurodevelopmental Disorders Panel Invitae United States | 404 | 241 |
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Invitae Overgrowth Syndromes Panel Invitae United States | 96 | 53 |
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Invitae Cystic Kidney Disease Panel Invitae United States | 96 | 44 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Invitae United States | 638 | 419 |
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Congenital Diaphragmatic Hernia Panel PreventionGenetics, part of Exact Sciences United States | 116 | 65 |
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PreventionGenetics, part of Exact Sciences United States | 41 | 38 |
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Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
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Top 99 Genetic Causes of Developmental Delay Panel PreventionGenetics, part of Exact Sciences United States | 170 | 99 |
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Invitae United States | 409 | 164 |
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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.