Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
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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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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 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Centogene AG - the Rare Disease Company Germany | 777 | 770 |
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Centogene AG - the Rare Disease Company Germany | 247 | 262 |
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Centogene AG - the Rare Disease Company Germany | 289 | 275 |
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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 971 | 680 |
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Invitae Neurodevelopmental Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 404 | 241 |
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Invitae Cerebral Palsy Spectrum Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 638 | 419 |
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Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
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Kleefstra syndrome, 610253, Autosomal dominant (Kleefstra syndrome) (440) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Kleefstra syndrome, 610253, Autosomal dominant (Kleefstra syndrome) (Prenatal) (440) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Top 99 Genetic Causes of Developmental Delay Panel PreventionGenetics, part of Exact Sciences United States | 170 | 99 |
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Quantitative Genomic Medicine Laboratories, SL Spain | 184 | 162 |
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Invitae Mendelian Disorders with Psychiatric Symptoms Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 254 | 166 |
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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.