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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
CLRN1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
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Centogene AG - the Rare Disease Company Germany | 203 | 194 |
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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 |
|
Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
|
Invitae Broad Carrier Screen without X-linked Disorders Invitae United States | 195 | 98 |
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Invitae United States | 224 | 112 |
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Invitae Comprehensive Carrier Screen Invitae United States | 886 | 547 |
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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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PreventionGenetics, part of Exact Sciences United States | 91 | 82 |
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Autosomal Recessive Retinitis Pigmentosa (RP) Panel PreventionGenetics, part of Exact Sciences United States | 62 | 60 |
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CLRN1 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 2 | 1 |
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CLRN1 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 2 | 1 |
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Baylor Genetics United States | 2 | 1 |
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Baylor Genetics United States | 842 | 637 |
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Retinitis pigmentosa 61 (sequence analysis of CLRN1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India | 376 | 317 |
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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.