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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
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Centogene AG - the Rare Disease Company Germany | 243 | 238 |
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Bone Marrow Failure / Anemia Panel Centogene AG - the Rare Disease Company Germany | 212 | 212 |
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Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 67 | 41 |
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Invitae Disorders of Sex Development Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 88 | 53 |
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SERKAL syndrome, 611812, Autosomal recessive (SERKAL syndrome) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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SERKAL syndrome, 611812, Autosomal recessive (SERKAL syndrome) (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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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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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 525 | 338 |
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PreventionGenetics, part of Exact Sciences United States | 128 | 85 |
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46,XX Differences of Sex Development (DSD) via the WNT4 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 2 | 1 |
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SERKAL syndrome: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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Fulgent Genetics United States | 79 | 45 |
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Müllerian Aplasia And Hyperandrogenism (WNT4 Single Gene Test) Fulgent Genetics United States | 2 | 1 |
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Fulgent Genetics United States | 92 | 56 |
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Fulgent Genetics United States | 76 | 41 |
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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.