Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
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CIB2 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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Invitae United States | 32 | 17 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 360 | 222 |
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Molecular Vision Laboratory United States | 342 | 268 |
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Usher Syndrome Type IJ and Deafness, Autosomal Recessive 48 (DFNB48) via the CIB2 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
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PreventionGenetics, part of Exact Sciences United States | 11 | 12 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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Usher syndrome type IJ (sequence analysis of CIB2 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Non-syndromic hearing loss panel. 95-gene NGS panel. Genologica Medica Spain | 146 | 94 |
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Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain | 420 | 257 |
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Autosomal recessive hearing loss. 41-gene NGS panel. Genologica Medica Spain | 65 | 41 |
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Usher Syndrome (NGS Panel and Copy Number Analysis) MNG Laboratories (Medical Neurogenetics, LLC.) United States | 10 | 12 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 2 | 1 |
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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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Usher syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 14 | 13 |
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