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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
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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High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
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aCGH study for cryptic quantitative genomic imbalances Institute of Human Genetics Foundation for Research in Genetics and Endocrinology India | 90 | 24 |
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Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
|
Michigan Medical Genetics Laboratories University of Michigan United States | 18 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Chromosome 2q37 deletion syndrome, 600430, Autosomal dominant (2q37 microdeletion syndrome) (440) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Amplexa Genetics Amplexa Genetics A/S Denmark | 1 | 1 |
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Cytogenetics Laboratory SUNY Upstate Medical University United States | 114 | 1 |
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Brachydactyly-mental retardation syndrome (sequence analysis of HDAC4 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
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Genolife InformaciĆ³n de Vida Mexico | 34 | 16 |
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Fulgent Genetics United States | 1 | 1 |
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Epilepsy Comprehensive NGS Panel Fulgent Genetics United States | 729 | 398 |
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Fulgent Genetics United States | 543 | 178 |
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Fulgent Genetics United States | 5128 | 4672 |
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Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
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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.