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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv4729700copy number variation1nstd102humanLikely benign GRCh37 chr11: 30,216,157-30,276,703 , GRCh38.p12 chr11: 30,194,610-30,255,156 FSHB, ARL14EP-DT
    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
    nsv4456492copy number variation1nstd102humanPathogenic GRCh37 chr11: 30,217,030-30,276,703 , GRCh38.p12 chr11: 30,195,483-30,255,156 ARL14EP-DT, FSHB
    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
    nsv4202384copy number variation1nstd166human GRCh37.p13 chr11: 30,210,781-30,270,027 , GRCh38.p12 chr11: 30,189,234-30,248,480 ARL14EP-DT, FSHB
    nsv4193647copy number variation1nstd166human GRCh37.p13 chr11: 30,250,575-30,255,897 , GRCh38.p12 chr11: 30,229,028-30,234,350 FSHB, ARL14EP-DT
    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
    nsv3915798copy number variation1nstd102humanPathogenic GRCh37 chr11: 24,616,945-31,118,086 , NCBI36 chr11: 24,573,521-31,074,662 , GRCh38 chr11: 24,595,399-31,096,539 LOC107987160, LOC105376604, 61 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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3908389copy number variation1nstd102humanPathogenic GRCh37 chr11: 25,771,208-35,614,978 , GRCh38.p12 chr11: 25,749,661-35,593,430 METTL15, LOC105376611, 128 more genes
    nsv3907223copy number variation1nstd102humanPathogenic GRCh37 chr11: 24,469,451-37,524,085 , GRCh38.p12 chr11: 24,447,905-37,502,535 PIGCP1, HNRNPRP2, 151 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3904666copy number variation1nstd102humanPathogenic GRCh37 chr11: 29,750,813-32,752,091 , GRCh38.p12 chr11: 29,729,266-32,730,545 LINC01616, LOC105376611, 34 more genes
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