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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    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
    nsv5303667copy number variation1nstd204human GRCh38.p13 chr11: 113,710,564-113,773,665 , GRCh37.p13 chr11: 113,581,286-113,644,387 ZW10, RPS29P19, 2 more genes
    nsv5280006copy number variation1nstd204human GRCh38.p13 chr11: 113,710,173-113,771,272 , GRCh37.p13 chr11: 113,580,895-113,641,994 LOC100288385, TMPRSS5, 3 more genes
    nsv5278713copy number variation1nstd204human GRCh38.p13 chr11: 113,738,153-113,739,152 , GRCh37.p13 chr11: 113,608,875-113,609,874 ZW10
    nsv5268108copy number variation1nstd204human GRCh38.p13 chr11: 113,771,201-113,772,500 , GRCh37.p13 chr11: 113,641,923-113,643,222 ZW10
    nsv5266993copy number variation1nstd204human GRCh38.p13 chr11: 113,711,601-113,774,600 , GRCh37.p13 chr11: 113,582,323-113,645,322 LOC100288385, RPS29P19, 2 more genes
    nsv5264524copy number variation1nstd204human GRCh38.p13 chr11: 113,748,228-113,756,678 , GRCh37.p13 chr11: 113,618,950-113,627,400 ZW10, RPS29P19
    nsv5181867mobile element insertion1nstd203human GRCh38 chr11: 113,755,638-113,755,655 , GRCh37.p13 chr11: 113,626,360-113,626,377 ZW10
    nsv4980740copy number variation1nstd200human GRCh38 chr11: 113,754,360-113,759,142 , GRCh37.p13 chr11: 113,625,082-113,629,864 ZW10
    nsv4837620copy number variation1nstd200human GRCh37 chr11: 113,581,290-113,644,383 , GRCh38.p12 chr11: 113,710,568-113,773,661 LOC100288385, RPS29P19, 2 more genes
    nsv4676058copy number variation1nstd102humanUncertain significance GRCh37 chr11: 113,441,348-113,645,902 , GRCh38.p12 chr11: 113,570,626-113,775,180 LOC100288385, TMPRSS5, 4 more genes
    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
    nsv4575862mobile element insertion1nstd166human GRCh37.p13 chr11: 113,626,360-113,626,360 , GRCh38.p12 chr11: 113,755,638-113,755,638 ZW10
    nsv4547471insertion1nstd166human GRCh37.p13 chr11: 113,611,064-113,611,064 , GRCh38.p12 chr11: 113,740,342-113,740,342 ZW10
    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
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3913577copy number variation1nstd102humanPathogenic NCBI36 chr11: 105,972,805-113,384,939 , GRCh37.p13 chr11: 106,467,595-113,879,729 , GRCh38.p12 chr11: 106,596,868-114,009,007 LAYN, DDX10, 133 more genes
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