Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
CRB1 - NGS including CNV analysis Centogene US, LLC - The Rare Disease Company United States | 3 | 1 |
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CRB1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Invitae Macular Dystrophy Panel Invitae United States | 66 | 36 |
|
PreventionGenetics United States | 285 | 137 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Intergen Genetic Diagnosis and Research Centre Turkey | 1 | 1 |
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Invitae Inherited Retinal Disorders Panel Invitae United States | 486 | 293 |
|
Molecular Vision Laboratory United States | 342 | 268 |
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Stargardt Disease (STGD) and Macular Dystrophies Panel PreventionGenetics United States | 35 | 28 |
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PreventionGenetics United States | 91 | 82 |
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Autosomal Dominant Retinitis Pigmentosa (RP) Panel PreventionGenetics United States | 32 | 30 |
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Autosomal Recessive Retinitis Pigmentosa (RP) Panel PreventionGenetics United States | 62 | 60 |
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Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC Netherlands | 3 | 1 |
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Leber Congential Amaurosis Panel (MitomeNGS) Baylor Genetics United States | 32 | 19 |
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Baylor Genetics United States | 3 | 1 |
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CRB1 Deletion/Duplication Analysis Baylor Genetics United States | 3 | 1 |
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CRB1 Comprehensive - Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 3 | 1 |
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CRB1 Sequence Analysis (Prenatal Diagnosis) Baylor Genetics United States | 3 | 1 |
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Baylor Genetics United States | 842 | 637 |
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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.