Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Baylor Genetics United States | 842 | 637 |
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Comprehensive Hearing Loss + mtDNA MNG Laboratories (Medical Neurogenetics, LLC.) United States | 218 | 300 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 2 | 1 |
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Peroxisomal disorders panel. NGS panel of 27 genes. Genologica Medica Spain | 45 | 27 |
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Peroxisomal Disorders Gene Panel Duzen Laboratories Duzen BBAGUAS Turkey | 39 | 30 |
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HSD17B4 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 2 | 1 |
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Asper Biogene Asper Biogene LLC Estonia | 85 | 64 |
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NxGen MDx United States | 116 | 117 |
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NxGen MDx United States | 113 | 115 |
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Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 184 |
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Perrault Syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 6 | 6 |
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Perrault Syndrome , Panel Massive Sequencing (NGS) 5 Genes Reference Laboratory Genetics Spain | 5 | 5 |
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Leukodystrophies , Panel Massive Sequencing (NGS) 57 genes Reference Laboratory Genetics Spain | 60 | 56 |
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Perrault Syndrome Type 1 , Sequencing HSD17B4 Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States | 198 | 157 |
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CeGaT GmbH Germany | 2 | 1 |
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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.