Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) Panel PreventionGenetics, part of Exact Sciences United States | 82 | 77 |
|
Inherited Loss of Hearing Panel Dhiti Omics Technologies Private Ltd India | 8 | 179 |
|
Cataract panel. NGS panel of 69 genes. Genologica Medica Spain | 146 | 69 |
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Branchial-Oto-Renal Syndrome Panel. Panel NGS genes: EYA1, SIX1, SIX5, TFAP2A. Genologica Medica Spain | 7 | 4 |
|
Kabuki syndrome panel. 7-gene NGS panel. Genologica Medica Spain | 16 | 7 |
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Renal malformation panel. NGS panel of 22 genes. Genologica Medica Spain | 44 | 22 |
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GeneDx United States | 56 | 150 |
|
Hearing Loss, Comprehensive Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 142 | 84 |
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Congenital Cataracts NGS Panel Fulgent Genetics United States | 106 | 56 |
|
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States | 223 | 83 |
|
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States | 332 | 167 |
|
Nonsyndromic Hearing Loss NGS Panel Fulgent Genetics United States | 146 | 99 |
|
Fulgent Genetics United States | 43 | 15 |
|
Fulgent Genetics United States | 17 | 7 |
|
Fulgent Genetics United States | 68 | 41 |
|
Branchiootorenal Spectrum Disorders NGS Panel Fulgent Genetics United States | 6 | 3 |
|
Asper Biogene Asper Biogene LLC Estonia | 12 | 7 |
|
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 184 |
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BOR SYNDROME (BRANCHIO-OTO-RENAL) Laboratorio de Genetica Clinica SL Spain | 3 | 3 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 135 | 136 |
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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.