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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6917712copy number variation1nstd229human GRCh38 chr11: 118,232,544-118,237,510 , GRCh37.p13 chr11: 118,103,259-118,108,225 MPZL3
    nsv6916879copy number variation1nstd229human GRCh38 chr11: 118,218,619-118,226,903 , GRCh37.p13 chr11: 118,089,334-118,097,618 MPZL3, JAML
    nsv6916307copy number variation1nstd229human GRCh38 chr11: 118,225,991-118,226,033 , GRCh37.p13 chr11: 118,096,706-118,096,748 MPZL3
    nsv6907747copy number variation1nstd229human GRCh38 chr11: 118,240,756-118,240,785 , GRCh37.p13 chr11: 118,111,471-118,111,500 MPZL3
    nsv6906561copy number variation1nstd229human GRCh38 chr11: 118,231,501-118,237,500 , GRCh37.p13 chr11: 118,102,216-118,108,215 MPZL3
    nsv6463643copy number variation1nstd223human GRCh38 chr11: 118,232,543-118,237,509 , GRCh37.p13 chr11: 118,103,258-118,108,224 MPZL3
    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
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 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
    nsv5924524copy number variation1nstd209human GRCh38 chr11: 118,239,575-118,241,480 , GRCh37.p13 chr11: 118,110,290-118,112,195 MPZL3
    nsv5856702copy number variation1nstd209human GRCh38 chr11: 118,239,900-118,241,801 , GRCh37.p13 chr11: 118,110,615-118,112,516 MPZL3
    nsv5712456mobile element insertion1nstd211human GRCh38 chr11: 118,250,195-118,250,195 , GRCh37.p13 chr11: 118,120,910-118,120,910 MPZL3
    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
    nsv5355485translocation1nstd200human GRCh38 chr11: 118,247,507-118,247,507 , GRCh38 chr18: 12,884,264-12,884,264 , GRCh37.p13 chr11: 118,118,222-118,118,222 , GRCh37.p13 chr18: 12,884,263-12,884,263 PTPN2, MPZL3
    nsv5343277translocation1nstd200human GRCh37 chr11: 118,118,222-118,118,222 , GRCh37 chr18: 12,884,263-12,884,263 , GRCh38.p12 chr11: 118,247,507-118,247,507 , GRCh38.p12 chr18: 12,884,264-12,884,264 MPZL3, PTPN2
    nsv5277535copy number variation1nstd204human GRCh38.p13 chr11: 118,250,494-118,252,617 , GRCh37.p13 chr11: 118,121,209-118,123,332 MPZL3, MPZL2
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