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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123890insertion1nstd186human GRCh37 chr11: 113,185,605-113,185,656 , GRCh38.p12 chr11: 113,314,883-113,314,934 TTC12
    nsv5728088mobile element insertion1nstd211human GRCh38 chr11: 113,332,051-113,332,051 , GRCh37.p13 chr11: 113,202,773-113,202,773 , GRCh37.p13 chr11|NW_003871078.1: 514,777-514,777 TTC12
    nsv5700287mobile element insertion1nstd211human GRCh38 chr11: 113,364,564-113,364,564 , GRCh37.p13 chr11: 113,235,286-113,235,286 TTC12
    nsv5541742insertion1nstd206human GRCh38 chr11: 113,314,883-113,314,934 , GRCh37.p13 chr11: 113,185,605-113,185,656 , GRCh37.p13 chr11|NW_003871078.1: 497,609-497,660 TTC12
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5416763mobile element insertion1nstd206human GRCh38 chr11: 113,364,564-113,364,615 , GRCh37.p13 chr11: 113,235,286-113,235,337 TTC12
    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
    nsv5180106mobile element insertion1nstd203human GRCh38 chr11: 113,332,033-113,332,051 , GRCh37.p13 chr11|NW_003871078.1: 514,759-514,777 , GRCh37.p13 chr11: 113,202,755-113,202,773 TTC12
    nsv4980726copy number variation1nstd200human GRCh38 chr11: 113,328,487-113,333,256 , GRCh37.p13 chr11: 113,199,209-113,203,978 , GRCh37.p13 chr11|NW_003871078.1: 511,213-515,982 TTC12
    nsv4723917insertion1nstd186human GRCh37 chr11: 113,185,579-113,185,579 , GRCh38.p12 chr11: 113,314,857-113,314,857 TTC12
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4557371mobile element insertion1nstd166human GRCh37.p13 chr11: 113,194,285-113,194,285 , GRCh38.p12 chr11: 113,323,563-113,323,563 TTC12
    nsv4552964insertion1nstd166human GRCh37.p13 chr11: 113,185,579-113,185,579 , GRCh38.p12 chr11: 113,314,857-113,314,857 TTC12
    nsv4503586mobile element insertion1nstd166human GRCh37.p13 chr11: 113,212,531-113,212,531 , GRCh38.p12 chr11: 113,341,809-113,341,809 TTC12
    nsv4456659copy number variation1nstd102humanUncertain significance GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787 RPS29P19, PPP2R1B, 95 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4205415copy number variation1nstd166human GRCh37.p13 chr11: 113,199,209-113,203,978 , GRCh38.p12 chr11: 113,328,487-113,333,256 TTC12
    nsv4204242copy number variation1nstd166human GRCh37.p13 chr11: 113,238,358-113,238,457 , GRCh38.p12 chr11: 113,367,636-113,367,735 TTC12
    nsv4203861copy number variation1nstd166human GRCh37.p13 chr11: 113,208,557-113,209,427 , GRCh38.p12 chr11: 113,337,835-113,338,705 TTC12
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