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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073698inversion1nstd229human GRCh38 chr11: 41,832,508-41,832,606 , GRCh37.p13 chr11: 41,854,058-41,854,156 LINC01499
    nsv7066550inversion1nstd229human GRCh38 chr11: 41,804,526-41,816,075 , GRCh37.p13 chr11: 41,826,076-41,837,625 LINC01499
    nsv7064640inversion1nstd229human GRCh38 chr11: 41,729,110-41,730,921 , GRCh37.p13 chr11: 41,750,660-41,752,471 LINC01499
    nsv7062837inversion1nstd229human GRCh38 chr11: 40,841,838-44,720,409 , GRCh37.p13 chr11: 40,863,388-44,741,959 TTC17, ACCSL, 35 more genes
    nsv6918032copy number variation1nstd229human GRCh38 chr11: 41,738,355-41,738,502 , GRCh37.p13 chr11: 41,759,905-41,760,052 LINC01499
    nsv6917720copy number variation1nstd229human GRCh38 chr11: 41,826,529-41,829,200 , GRCh37.p13 chr11: 41,848,079-41,850,750 LINC01499
    nsv6917526copy number variation1nstd229human GRCh38 chr11: 41,763,978-41,786,279 , GRCh37.p13 chr11: 41,785,528-41,807,829 LINC01499
    nsv6915523copy number variation1nstd229human GRCh38 chr11: 41,802,232-41,820,187 , GRCh37.p13 chr11: 41,823,782-41,841,737 LINC01499
    nsv6912894copy number variation1nstd229human GRCh38 chr11: 41,833,874-41,904,692 , GRCh37.p13 chr11: 41,855,424-41,926,242 LOC105376639, LINC01499
    nsv6912428copy number variation1nstd229human GRCh38 chr11: 41,763,401-41,765,700 , GRCh37.p13 chr11: 41,784,951-41,787,250 LINC01499
    nsv6911783copy number variation1nstd229human GRCh38 chr11: 41,800,739-41,801,066 , GRCh37.p13 chr11: 41,822,289-41,822,616 LINC01499
    nsv6910702copy number variation1nstd229human GRCh38 chr11: 41,709,201-41,730,400 , GRCh37.p13 chr11: 41,730,751-41,751,950 LINC01499, LINC02741
    nsv6910092copy number variation1nstd229human GRCh38 chr11: 41,790,690-41,808,824 , GRCh37.p13 chr11: 41,812,240-41,830,374 LINC01499
    nsv6907768copy number variation1nstd229human GRCh38 chr11: 41,781,737-41,781,838 , GRCh37.p13 chr11: 41,803,287-41,803,388 LINC01499
    nsv6907744copy number variation1nstd229human GRCh38 chr11: 41,733,443-41,733,619 , GRCh37.p13 chr11: 41,754,993-41,755,169 LINC01499
    nsv6907323copy number variation1nstd229human GRCh38 chr11: 41,572,638-42,754,333 , GRCh37.p13 chr11: 41,594,188-42,775,883 LOC105376642, LINC02745, 5 more genes
    nsv6905074copy number variation1nstd229human GRCh38 chr11: 41,803,006-41,803,185 , GRCh37.p13 chr11: 41,824,556-41,824,735 LINC01499
    nsv6905023copy number variation1nstd229human GRCh38 chr11: 41,814,917-41,815,040 , GRCh37.p13 chr11: 41,836,467-41,836,590 LINC01499
    nsv6904214copy number variation1nstd229human GRCh38 chr11: 41,796,648-41,797,475 , GRCh37.p13 chr11: 41,818,198-41,819,025 LINC01499
    nsv6902889copy number variation1nstd229human GRCh38 chr11: 41,766,136-41,774,768 , GRCh37.p13 chr11: 41,787,686-41,796,318 LINC01499
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