Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
CACNA1H Gene Epilepsy, childhood absence type 6, susceptibility to NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Comprehensive Nephrology Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 299 |
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Invitae Expanded Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 693 | 388 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 734 | 744 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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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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Invitae Progressive Renal Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 310 | 195 |
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Genomic Unity Epilepsy Analysis (includes STR analysis of 6 loci) Variantyx, Inc. United States | 1 | 378 |
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Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine United States | 525 | 338 |
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Primary Aldosteronism via the CACNA1H Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 4 | 4 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
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Genomic Unity® Renal Disorders Analysis Variantyx, Inc. United States | 1 | 425 |
|
CGC Genetics Unilabs Portugal | 1 | 759 |
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Hypertension (WES based NGS panel of 15 genes, including CNV analysis) CGC Genetics Unilabs Portugal | 1 | 15 |
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CGC Genetics Unilabs Portugal | 1 | 1 |
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FAMILIAL HYPERALDOSTERONISM TYPE IV. Complete sequencing by NGS Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 696 |
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