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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Molecular Vision Laboratory United States | 1358 | 1028 |
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EDNRB - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States | 297 | 180 |
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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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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
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PreventionGenetics, part of Exact Sciences United States | 39 | 33 |
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Waardenburg syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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Waardenburg syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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Waardenburg syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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PreventionGenetics, part of Exact Sciences United States | 12 | 6 |
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Hirschsprung Disease 2 (HSCR2) via the EDNRB Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
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Waardenburg Syndrome Type IVA via the EDNRB Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
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Craniosynostosis panel. NGS panel of 37 genes. Genologica Medica Spain | 113 | 37 |
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Mitochondrial genome sequencing Molecular Vision Laboratory United States | 526 | 339 |
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Waardenburg syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 10 | 7 |
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Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
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Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
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Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 184 |
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