Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
HSPD1 Gene SPG13 NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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HSD3B7 Gene Bile acid synthesis defect type 1, congenital NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
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HSD3B7 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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Centogene AG - the Rare Disease Company Germany | 669 | 688 |
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Centogene AG - the Rare Disease Company Germany | 498 | 498 |
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Centogene AG - the Rare Disease Company Germany | 499 | 499 |
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Centogene AG - the Rare Disease Company Germany | 829 | 848 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 210 | 134 |
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Labcorp Genetics (formerly Invitae) LabCorp United States | 173 | 119 |
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Mayo Clinic Laboratories Mayo Clinic United States | 7 | 112 |
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PreventionGenetics, part of Exact Sciences United States | 130 | 69 |
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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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Translational Metabolic Laboratory Radboud University Medical Centre Netherlands | 1 | 625 |
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Next Generation Sequencing for Jaundice Associated Genes Variation Test National Taiwan University Hospital A1 Center National Taiwan University Hospital Taiwan | 4 | 73 |
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Congenital Bile Acid Synthesis Defect Type 1 via the HSD3B7 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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Bile acid synthesis defect, congenital 1 (HSD3B7 gene) Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD Netherlands | 1 | 1 |
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CGC Genetics Unilabs Portugal | 1 | 837 |
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Movement diseases (WES based NGS panel of 931 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 10 | 930 |
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Congenital bile acid synthesis defect type 1 (sequence analysis of HSD3B7 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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