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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978830insertion1nstd209human GRCh38 chr11: 76,619,300-76,619,300 , GRCh37.p13 chr11: 76,330,344-76,330,344 LINC02757
    nsv5917602copy number variation1nstd209human GRCh38 chr11: 76,607,318-76,607,416 , GRCh37.p13 chr11: 76,318,362-76,318,460 LINC02757
    nsv5909857copy number variation1nstd209human GRCh38 chr11: 76,608,202-76,608,267 , GRCh37.p13 chr11: 76,319,246-76,319,311 LINC02757
    nsv5697657mobile element insertion1nstd211human GRCh38 chr11: 76,606,904-76,606,904 , GRCh37.p13 chr11: 76,317,948-76,317,948 LINC02757
    nsv5662266insertion2nstd207human GRCh38 chr11: 76,619,300-76,619,300 , GRCh37.p13 chr11: 76,330,344-76,330,344 LINC02757
    nsv5587804copy number variation1nstd207human GRCh38 chr11: 76,607,323-76,607,420 , GRCh37.p13 chr11: 76,318,367-76,318,464 LINC02757
    nsv5499460copy number variation1nstd206human GRCh38 chr11: 76,607,318-76,607,422 , GRCh37.p13 chr11: 76,318,362-76,318,466 LINC02757
    nsv5498703copy number variation1nstd206human GRCh38 chr11: 76,608,202-76,608,268 , GRCh37.p13 chr11: 76,319,246-76,319,312 LINC02757
    nsv5406879mobile element insertion1nstd206human GRCh38 chr11: 76,606,904-76,606,955 , GRCh37.p13 chr11: 76,317,948-76,317,999 LINC02757
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5309612copy number variation1nstd204human GRCh38.p13 chr11: 76,607,308-76,607,431 , GRCh37.p13 chr11: 76,318,352-76,318,475 LINC02757
    nsv4987384copy number variation1nstd200human GRCh38 chr11: 76,626,495-76,629,021 , GRCh37.p13 chr11: 76,337,539-76,340,065 LINC02757
    nsv4987383copy number variation1nstd200human GRCh38 chr11: 76,586,545-76,728,785 , GRCh37.p13 chr11: 76,297,589-76,439,829 , LRRC32, 2 more genes
    nsv4758131insertion1nstd199human GRCh37 chr11: 76,330,343-76,330,343 , GRCh38.p12 chr11: 76,619,299-76,619,299 LINC02757
    nsv4675349copy number variation1nstd102humanUncertain significance GRCh37 chr11: 76,238,742-76,537,128 , GRCh38.p12 chr11: 76,527,698-76,826,084 LRRC32, LINC02757, 5 more genes
    nsv4528176copy number variation1nstd166human GRCh37.p13 chr11: 76,318,362-76,318,466 , GRCh38.p12 chr11: 76,607,318-76,607,422 LINC02757
    nsv4480635mobile element insertion1nstd166human GRCh37.p13 chr11: 76,332,204-76,332,204 , GRCh38.p12 chr11: 76,621,160-76,621,160 LINC02757
    nsv4377601copy number variation1nstd173human GRCh37 chr11: 76,309,546-76,338,834 , GRCh38.p12 chr11: 76,598,502-76,627,790 LINC02757
    nsv4201343copy number variation1nstd166human GRCh37.p13 chr11: 76,337,539-76,340,065 , GRCh38.p12 chr11: 76,626,495-76,629,021 LINC02757
    nsv4197114copy number variation1nstd166human GRCh37.p13 chr11: 76,319,246-76,319,312 , GRCh38.p12 chr11: 76,608,202-76,608,268 LINC02757
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