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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6916387copy number variation1nstd229human GRCh38 chr11: 124,202,917-124,261,436 , GRCh37.p13 chr11: 124,073,624-124,131,332 OR8G7P, OR8G3P, 4 more genes
    nsv6914046copy number variation1nstd229human GRCh38 chr11: 124,203,265-124,243,357 , GRCh37.p13 chr11: 124,073,972-124,114,105 LOC102724410, OR8G2P, 3 more genes
    nsv6898470copy number variation1nstd229human GRCh38 chr11: 124,224,728-124,517,025 , GRCh37.p13 chr11: 124,095,433-124,386,921 OR8C1P, SLC5A4P1, 21 more genes
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6584901inversion1nstd223human GRCh38 chr11: 120,551,312-124,267,280 , GRCh37.p13 chr11: 120,422,021-124,137,176 RNU6-256P, CLMP, 85 more genes
    nsv6464655copy number variation1nstd223human GRCh38 chr11: 124,214,879-124,224,779 , GRCh37.p13 chr11: 124,085,586-124,095,484 LOC102724410, OR8G2P, 1 more genes
    nsv6462587copy number variation1nstd223human GRCh38 chr11: 124,222,001-124,222,900 , GRCh37.p13 chr11: 124,092,709-124,093,608 OR8G2P, LOC102724410
    nsv6459453copy number variation1nstd223human GRCh38 chr11: 124,225,572-124,265,772 , GRCh37.p13 chr11: 124,096,277-124,135,668 OR8G1, OR8G2P, 3 more genes
    nsv6459035copy number variation1nstd223human GRCh38 chr11: 124,208,803-124,225,728 , GRCh37.p13 chr11: 124,079,510-124,096,433 OR8G3P, LOC102724410, 1 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6143770copy number variation1nstd206human GRCh38 chr11: 124,224,861-124,225,014 , GRCh37.p13 chr11: 124,095,566-124,095,719 OR8G2P, LOC102724410
    nsv6025176copy number variation1nstd212human GRCh38 chr11: 124,214,763-124,224,764 , GRCh37.p13 chr11: 124,085,470-124,095,469 OR8G2P, OR8G3P, 1 more genes
    nsv5924780copy number variation1nstd209human GRCh38 chr11: 124,225,014-124,238,662 , GRCh37.p13 chr11: 124,095,719-124,109,403 OR8G2P, OR8G7P, 1 more genes
    nsv5907917copy number variation1nstd209human GRCh38 chr11: 124,208,803-124,225,727 , GRCh37.p13 chr11: 124,079,510-124,096,432 LOC102724410, OR8G3P, 1 more genes
    nsv5866006copy number variation1nstd209human GRCh38 chr11: 124,215,155-124,224,904 , GRCh37.p13 chr11: 124,085,862-124,095,609 OR8G3P, LOC102724410, 1 more genes
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