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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074850inversion1nstd229human GRCh38 chr10: 70,747,833-70,747,857 , GRCh37.p13 chr10: 72,507,589-72,507,613 ADAMTS14
    nsv7068862inversion1nstd229human GRCh38 chr10: 70,666,101-70,672,093 , GRCh37.p13 chr10: 72,425,857-72,431,849 ADAMTS14
    nsv6897056copy number variation1nstd229human GRCh38 chr10: 70,667,501-70,675,175 , GRCh37.p13 chr10: 72,427,257-72,434,931 ADAMTS14
    nsv6896225copy number variation1nstd229human GRCh38 chr10: 70,694,281-70,703,225 , GRCh37.p13 chr10: 72,454,037-72,462,981 ADAMTS14
    nsv6895523copy number variation1nstd229human GRCh38 chr10: 70,754,452-70,756,415 , GRCh37.p13 chr10: 72,514,208-72,516,171 ADAMTS14
    nsv6890444copy number variation1nstd229human GRCh38 chr10: 70,709,577-70,720,615 , GRCh37.p13 chr10: 72,469,333-72,480,371 ADAMTS14
    nsv6888956copy number variation1nstd229human GRCh38 chr10: 70,740,615-70,744,037 , GRCh37.p13 chr10: 72,500,371-72,503,793 ADAMTS14
    nsv6888792copy number variation1nstd229human GRCh38 chr10: 70,679,533-70,722,290 , GRCh37.p13 chr10: 72,439,289-72,482,046 ADAMTS14
    nsv6888187copy number variation1nstd229human GRCh38 chr10: 70,686,601-70,691,600 , GRCh37.p13 chr10: 72,446,357-72,451,356 ADAMTS14
    nsv6884082copy number variation1nstd229human GRCh38 chr10: 70,721,534-70,723,973 , GRCh37.p13 chr10: 72,481,290-72,483,729 ADAMTS14
    nsv6883703copy number variation1nstd229human GRCh38 chr10: 70,747,575-70,751,621 , GRCh37.p13 chr10: 72,507,331-72,511,377 ADAMTS14
    nsv6881416copy number variation1nstd229human GRCh38 chr10: 70,751,320-70,756,567 , GRCh37.p13 chr10: 72,511,076-72,516,323 ADAMTS14
    nsv6879831copy number variation1nstd229human GRCh38 chr10: 70,650,485-70,673,919 , GRCh37.p13 chr10: 72,410,241-72,433,675 ADAMTS14
    nsv6878818copy number variation1nstd229human GRCh38 chr10: 70,672,240-70,674,842 , GRCh37.p13 chr10: 72,431,996-72,434,598 ADAMTS14
    nsv6620675copy number variation1nstd224human GRCh37 chr10: 72,012,813-73,062,048 , GRCh38.p12 chr10: 70,253,057-71,302,291 ADAMTS14, TBATA, 17 more genes
    nsv6620606copy number variation1nstd224human GRCh37 chr10: 72,109,893-72,996,234 , GRCh38.p12 chr10: 70,350,137-71,236,477 NODAL, PCBD1, 15 more genes
    nsv6449794copy number variation1nstd223human GRCh38 chr10: 70,688,984-70,691,578 , GRCh37.p13 chr10: 72,448,740-72,451,334 ADAMTS14
    nsv6446380copy number variation1nstd223human GRCh38 chr10: 70,751,320-70,756,561 , GRCh37.p13 chr10: 72,511,076-72,516,317 ADAMTS14
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