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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
GENETIX Centro de Investigación en Genética Humana y Reproductiva Colombia | 6 | 1 |
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FGFR3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 14 | 1 |
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PreventionGenetics United States | 285 | 137 |
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Invitae Limb and Digital Malformations Panel Invitae United States | 356 | 177 |
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Non-Immune Hydrops Fetalis Panel PreventionGenetics United States | 291 | 148 |
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Polydactyly and Syndactyly Panel PreventionGenetics United States | 320 | 231 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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PreventionGenetics United States | 220 | 128 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 64 | 23 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 110 | 45 |
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PreventionGenetics United States | 177 | 163 |
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Hereditary Hearing Loss and Deafness Panel PreventionGenetics United States | 356 | 211 |
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Overgrowth and Macrocephaly Syndromes Panel PreventionGenetics United States | 150 | 88 |
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PreventionGenetics United States | 156 | 73 |
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HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
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Craniosynostosis Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
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Craniosynostosis Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 31 | 26 |
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Facial Dysostosis Related Disorders Panel PreventionGenetics United States | 33 | 19 |
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Craniosynostosis and Related Disorders Panel PreventionGenetics United States | 19 | 5 |
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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.