Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
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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Usher syndrome, type 2A, 276901, Autosomal recessive (Usher syndrome) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Otogenetics Usher Multi-Gene NGS Panel Otogenetics United States | 10 | 10 |
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GeneID Lab - Advanced Molecular Diagnostics United States | 73 | 61 |
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Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel Otogenetics United States | 122 | 128 |
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Molecular Vision Laboratory United States | 1358 | 1028 |
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Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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USH2A - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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PDZD7 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 405 | 219 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 32 | 17 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 16 | 9 |
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Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
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Invitae Broad Carrier Screen without X-linked Disorders Labcorp Genetics (formerly Invitae) LabCorp United States | 195 | 98 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 224 | 112 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 6 | 7 |
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Invitae Comprehensive Carrier Screen Labcorp Genetics (formerly Invitae) LabCorp United States | 886 | 547 |
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Myriad Genetics, Inc. United States | 2 | 1 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 362 | 227 |
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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.