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Items: 1 to 20 of 447

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907044copy number variation1nstd209human GRCh38 chr5: 10,756,068-10,756,402 , GRCh37.p13 chr5: 10,756,180-10,756,514 DAP
    nsv5899032copy number variation1nstd209human GRCh38 chr5: 10,679,786-10,679,848 , GRCh37.p13 chr5: 10,679,898-10,679,960 DAP
    nsv5895116copy number variation1nstd209human GRCh38 chr5: 10,681,224-10,681,399 , GRCh37.p13 chr5: 10,681,336-10,681,511 DAP
    nsv5888791copy number variation1nstd209human GRCh38 chr5: 10,681,361-10,681,613 , GRCh37.p13 chr5: 10,681,473-10,681,725 DAP
    nsv5718563mobile element insertion2nstd211human GRCh38 chr5: 10,749,372-10,749,372 , GRCh37.p13 chr5: 10,749,484-10,749,484 DAP
    nsv5637696insertion1nstd207human GRCh38 chr5: 10,730,758-10,730,758 , GRCh37.p13 chr5: 10,730,870-10,730,870 DAP
    nsv5636946insertion1nstd207human GRCh38 chr5: 10,681,696-10,681,696 , GRCh37.p13 chr5: 10,681,808-10,681,808 DAP
    nsv5627260insertion1nstd207human GRCh38 chr5: 10,730,486-10,730,486 , GRCh37.p13 chr5: 10,730,598-10,730,598 DAP
    nsv5584388copy number variation1nstd207human GRCh38 chr5: 10,756,068-10,756,402 , GRCh37.p13 chr5: 10,756,180-10,756,514 DAP
    nsv5582901copy number variation1nstd207human GRCh38 chr5: 10,730,506-10,730,603 , GRCh37.p13 chr5: 10,730,618-10,730,715 DAP
    nsv5471312copy number variation1nstd206human GRCh38 chr5: 10,756,070-10,756,403 , GRCh37.p13 chr5: 10,756,182-10,756,515 DAP
    nsv5381771copy number variation1nstd102humanPathogenic GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716 OTULINL, AKTIPP2, 317 more genes
    nsv5300856copy number variation1nstd204human GRCh38.p13 chr5: 10,756,070-10,756,403 , GRCh37.p13 chr5: 10,756,182-10,756,515 DAP
    nsv5239514copy number variation1nstd204human GRCh38.p13 chr5: 10,730,413-10,733,053 , GRCh37.p13 chr5: 10,730,525-10,733,165 DAP
    nsv5237580copy number variation1nstd204human GRCh38.p13 chr5: 10,756,101-10,756,400 , GRCh37.p13 chr5: 10,756,213-10,756,512 DAP
    nsv5188635mobile element insertion1nstd203human GRCh38 chr5: 10,749,357-10,749,370 , GRCh37.p13 chr5: 10,749,469-10,749,482 DAP
    nsv5084121mobile element insertion1nstd203human GRCh38 chr5: 10,691,716-10,691,731 , GRCh37.p13 chr5: 10,691,828-10,691,843 DAP
    nsv4946492copy number variation1nstd200human GRCh38 chr5: 10,756,070-10,756,403 , GRCh37.p13 chr5: 10,756,182-10,756,515 DAP
    nsv4946491copy number variation1nstd200human GRCh38 chr5: 10,728,286-10,728,365 , GRCh37.p13 chr5: 10,728,398-10,728,477 DAP
    nsv4946490copy number variation1nstd200human GRCh38 chr5: 10,719,743-10,722,317 , GRCh37.p13 chr5: 10,719,855-10,722,429 DAP
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