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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975770insertion1nstd209human GRCh38 chr11: 33,740,546-33,740,546 , GRCh37.p13 chr11: 33,762,092-33,762,092 FBXO3
    nsv5508007copy number variation1nstd206human GRCh38 chr11: 33,745,912-33,746,127 , GRCh37.p13 chr11: 33,767,458-33,767,673 FBXO3
    nsv5507448copy number variation1nstd206human GRCh38 chr11: 33,761,646-33,761,703 , GRCh37.p13 chr11: 33,783,192-33,783,249 FBXO3
    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
    nsv5320267copy number variation1nstd204human GRCh37.p13 chr11: 33,794,346-33,801,991 , GRCh38.p13 chr11: 33,772,800-33,780,445 FBXO3, FBXO3-DT
    nsv4986998copy number variation1nstd200human GRCh38 chr11: 33,772,804-33,780,443 , GRCh37.p13 chr11: 33,794,350-33,801,989 FBXO3-DT, FBXO3
    nsv4840742copy number variation1nstd200human GRCh37 chr11: 33,794,350-33,801,989 , GRCh38.p12 chr11: 33,772,804-33,780,443 FBXO3-DT, FBXO3
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675518copy number variation1nstd102humanUncertain significance GRCh37 chr11: 33,221,821-34,569,417 , GRCh38.p12 chr11: 33,200,275-34,547,870 HIPK3, C11orf91, 20 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4495779mobile element insertion1nstd166human GRCh37.p13 chr11: 33,766,537-33,766,537 , GRCh38.p12 chr11: 33,744,991-33,744,991 FBXO3
    nsv4483480mobile element insertion1nstd166human GRCh37.p13 chr11: 33,790,075-33,790,075 , GRCh38.p12 chr11: 33,768,529-33,768,529 FBXO3
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv4204114copy number variation1nstd166human GRCh37.p13 chr11: 33,785,190-33,786,101 , GRCh38.p12 chr11: 33,763,644-33,764,555 FBXO3
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3922664copy number variation1nstd102humanPathogenic GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709 CSTF3, LOC101928338, 170 more genes
    nsv3910889copy number variation1nstd102humanPathogenic GRCh38 chr11: 26,368,962-35,252,976 , NCBI36 chr11: 26,347,085-35,231,099 , GRCh37 chr11: 26,390,509-35,274,523 WT1, LOC105376611, 122 more genes
    nsv3909118copy number variation1nstd102humanPathogenic GRCh37 chr11: 29,883,001-33,865,721 , GRCh38.p12 chr11: 29,861,454-33,844,175 LOC101928338, PAUPAR, 56 more genes
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