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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
UPF3B - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
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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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Invitae Connective Tissue Disorders Panel Invitae United States | 195 | 92 |
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Invitae Overgrowth Syndromes Panel Invitae United States | 96 | 53 |
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Autism Spectrum Disorders (ASD) Panel PreventionGenetics, part of Exact Sciences United States | 224 | 170 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
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Overgrowth and Macrocephaly Syndromes Panel PreventionGenetics, part of Exact Sciences United States | 145 | 112 |
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Intellectual Disability (Syndromic and Non-Syndromic) via the UPF3B Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
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X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences United States | 191 | 141 |
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X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
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Marfan syndrome panel. 30-gene NGS panel. Genologica Medica Spain | 71 | 30 |
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X-linked intellectual disability panel. 99-gene NGS panel. Genologica Medica Spain | 143 | 99 |
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Macrocephaly / overgrowth syndrome panel. 43-gene NGS panel. Genologica Medica Spain | 88 | 43 |
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Intellectual Disability X-linked Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 136 | 90 |
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Intellectual Disability & Autism Spectrum Disorders Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 210 | 139 |
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Institute for Human Genetics University Medical Center Freiburg Germany | 1 | 1 |
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Mental retardation, X-linked syndromic: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 33 | 31 |
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Macrocephaly/Overgrowth Syndrome NGS Panel Fulgent Genetics United States | 100 | 38 |
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