Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
DIAPH3 Gene Auditory neuropathy, autosomal dominant NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
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Genomic Unity® Hearing Loss Disorders Analysis Variantyx, Inc. United States | 1 | 318 |
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AudioloGene Hearing Loss Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 200 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 405 | 219 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 362 | 227 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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Deafness or hypoacusis panel_v.2.0 CGC Genetics Unilabs Portugal | 1 | 272 |
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Auditory neuropathy 1 AD (sequence analysis of DIAPH3 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Inherited Loss of Hearing Panel Dhiti Omics Technologies Private Ltd India | 8 | 179 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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GeneDx United States | 56 | 150 |
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Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 137 |
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Auditory neuropathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 4 | 3 |
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Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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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.