Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics United States | 287 | 218 |
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High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
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Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
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Molecular Vision Laboratory United States | 1358 | 1028 |
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SOX10 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 3 | 1 |
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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
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Invitae Hypogonadotropic Hypogonadism Panel Invitae United States | 67 | 46 |
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Invitae Hypopigmentation Panel Invitae United States | 83 | 46 |
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Invitae Comprehensive Deafness Panel Invitae United States | 405 | 219 |
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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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Hereditary Hearing Loss and Deafness Panel PreventionGenetics, part of Exact Sciences United States | 361 | 224 |
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PreventionGenetics, part of Exact Sciences United States | 128 | 85 |
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Waardenburg syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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Waardenburg syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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Waardenburg syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States | 8 | 7 |
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PreventionGenetics, part of Exact Sciences United States | 12 | 6 |
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Waardenburg Syndrome Types IIE and IVC via the SOX10 Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
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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 | 3 | 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.