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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
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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Molecular Vision Laboratory United States | 1358 | 1028 |
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ARSG - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 417 | 413 |
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Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 405 | 219 |
|
Labcorp Genetics (formerly Invitae) LabCorp United States | 32 | 17 |
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Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 362 | 227 |
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PreventionGenetics, part of Exact Sciences United States | 11 | 12 |
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Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
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CGC Genetics Unilabs Portugal | 1 | 203 |
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CGC Genetics Unilabs Portugal | 1 | 306 |
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CGC Genetics Unilabs Portugal | 1 | 837 |
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Síndrome de Usher (WES based NGS panel of 13 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 13 |
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Lysosomal and peroxisomal diseases (WES based NGS panel of 122 genes, including analysis of CNVs) CGC Genetics Unilabs Portugal | 1 | 122 |
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Usher syndrome type 4 (sequence analysis of ARSG gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Mendelics Brazil | 1 | 321 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Xpanded Adult Movement Disorders Panel GeneDx United States | 5 | 473 |
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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.