Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
STRADA Gene Polyhydramnios, megalencephaly, and symptomatic epilepsy NGS Genetic DNA Test DNA Labs India India | 1 | 1 |
|
Comprehensive Epilepsy Gene Panel Mayo Clinic Laboratories Mayo Clinic United States | 1 | 318 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
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Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel Invitae United States | 971 | 680 |
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Invitae Overgrowth Syndromes Panel Invitae United States | 96 | 53 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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qGenEx Intellectual disability Quantitative Genomic Medicine Laboratories, SL Spain | 3 | 1969 |
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Genomic Unity Epilepsy Analysis (includes STR analysis of 6 loci) Variantyx, Inc. United States | 1 | 378 |
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Overgrowth and Macrocephaly Syndromes Panel PreventionGenetics, part of Exact Sciences United States | 145 | 112 |
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Invitae United States | 466 | 297 |
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Genetic Services Laboratory University of Chicago United States | 26 | 68 |
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Baylor Genetics United States | 1 | 397 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
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CGC Genetics Unilabs Portugal | 1 | 832 |
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CGC Genetics Unilabs Portugal | 1 | 1293 |
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Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
|
Mendelics Brazil | 1 | 240 |
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HEREDITARY ATAXIAS EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 1202 |
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Laboratorio de Genetica Clinica SL Spain | 1 | 696 |
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MACROCEPHALY AND OVERGROWTH SYNDROMES EXOME PANEL Laboratorio de Genetica Clinica SL Spain | 1 | 80 |
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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.