Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Fragile X Syndrome, Repeat Number Analysis with Reflex to Methylation Analysis Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital United States | 6 | 1 |
|
Center for Genetics at Saint Francis Saint Francis Hospital United States | 1 | 1 |
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Genetics Laboratory Shodair Children's Hospital United States | 1 | 1 |
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Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 185 | 145 |
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Carrier Screening - Fragile X Syndrome (FMR1) Genesys Diagnostics Genesys Diagnostics, Inc. United States | 3 | 1 |
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Fragile X Syndrome, Mol. Analysis Mayo Clinic Laboratories Mayo Clinic United States | 4 | 1 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Fragile X syndrome (FMR1 gene) Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS Chile | 1 | 1 |
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EPISign Whole Genome Methylation Assay Molecular Genetics Laboratory London Health Sciences Centre Canada | 19 | 1 |
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GeneID Lab - Advanced Molecular Diagnostics United States | 73 | 61 |
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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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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Asuragen Clinical Laboratory Asuragen, Inc United States | 2 | 1 |
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fragile-X syndrome molecular diagnostics Laboratoire de Diagnostic Moleculaire Hopital Saint-Francois d'Assise du CHU de Québec UL Canada | 1 | 1 |
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Invitae FMR1-Fragile X Syndrome and Related Disorders Repeat Expansion Test Invitae United States | 3 | 1 |
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Invitae United States | 3 | 1 |
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Genomic Unity® Genome-wide CNV and FMR1 Analysis Variantyx, Inc. United States | 5 | 2 |
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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.