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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Vision Laboratory United States | 1358 | 1028 |
|
TEAD1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Invitae Inherited Retinal Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 486 | 293 |
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Molecular Vision Laboratory United States | 342 | 268 |
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Genomic Unity® Retinal Disorders Analysis Variantyx, Inc. United States | 1 | 394 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
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CGC Genetics Unilabs Portugal | 1 | 306 |
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CGC Genetics Unilabs Portugal | 1 | 223 |
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Diseases of the posterior ocular segment (WES based NGS panel of 307 gene, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 307 |
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Aicardi syndrome (sequence analysis of TEAD1 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Mendelics Brazil | 1 | 321 |
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HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
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Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine United States | 1 | 695 |
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Retinal dystrophy panel. 260 gene NGS panel. Genologica Medica Spain | 420 | 257 |
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Genomic Unity® Custom Analysis Variantyx, Inc. United States | 1 | 4054 |
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Sarcoma Comprehensive NGS Fusion Panel NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States | 1 | 97 |
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GeneDx United States | 1 | 999 |
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Retinopathy and Optic Atrophy NGS Panel Fulgent Genetics United States | 563 | 241 |
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Eye diseases comprehensive panel Asper Biogene Asper Biogene LLC Estonia | 367 | 291 |
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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.