Filters
reset allTests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 288 | 218 |
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GJB6 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 4 | 1 |
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Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 164 |
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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 | 360 | 222 |
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Molecular Diagnostics Children's Hospital of Wisconsin United States | 9 | 5 |
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PreventionGenetics, part of Exact Sciences United States | 4 | 1 |
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Ectodermal dysplasia panel. 23-gene NGS panel. Genologica Medica Spain | 60 | 23 |
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Autosomal Dominant Hearing Loss. 25-gene NGS panel. Genologica Medica Spain | 48 | 23 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
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Palmoplantar keratoderma panel. 25-gene NGS panel. Genologica Medica Spain | 62 | 25 |
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Autosomal recessive hearing loss. 41-gene NGS panel. Genologica Medica Spain | 65 | 41 |
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Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 10 | 2 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 4 | 1 |
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Deafness, autosomal recessive: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 75 | 75 |
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Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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Fulgent Genetics United States | 98 | 43 |
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Nonsyndromic Hearing Loss NGS Panel Fulgent Genetics United States | 146 | 99 |
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Clouston Syndrome (GJB6 Single Gene Test) Fulgent Genetics United States | 5 | 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.