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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5659927insertion1nstd207human GRCh38 chr11: 1,754,533-1,754,533 , GRCh37.p13 chr11: 1,775,763-1,775,763 CTSD
    nsv5499592copy number variation1nstd206human GRCh38 chr11: 1,387,775-1,884,405 , GRCh37.p13 chr11: 1,409,005-1,905,635 , MOB2, 24 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5380721copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 1,774,733-1,785,089 , GRCh38.p12 chr11: 1,753,503-1,763,859 CTSD
    nsv5354654translocation1nstd200human GRCh38 chr11: 1,757,745-1,757,745 , GRCh38 chr11: 1,757,580-1,757,580 , GRCh37.p13 chr11: 1,778,810-1,778,810 , GRCh37.p13 chr11: 1,778,975-1,778,975 CTSD
    nsv4984130copy number variation1nstd200human GRCh38 chr11: 1,716,430-1,797,665 , GRCh37.p13 chr11: 1,737,660-1,818,895 RPL36AP39, CTSD, 2 more genes
    nsv4977857copy number variation1nstd200human GRCh38 chr11: 1,728,035-1,781,335 , GRCh37.p13 chr11: 1,749,265-1,802,565 LOC105376517, IFITM10, 1 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4757829insertion1nstd199human GRCh37 chr11: 1,775,607-1,775,607 , GRCh38.p12 chr11: 1,754,377-1,754,377 CTSD
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4729545copy number variation1nstd102humanPathogenic GRCh37 chr11: 1,436,158-2,321,134 , GRCh38.p12 chr11: 1,414,928-2,299,904 MIR4686, H19, 40 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 more genes
    nsv4681514copy number variation2nstd102humanUncertain significance GRCh37 chr11: 612,625-2,193,840 , GRCh38.p12 chr11: 612,625-2,172,610 LINC02688, TNNI2, 74 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
    nsv4599749copy number variation1nstd183human GRCh37 chr11: 1,760,556-1,841,827 , GRCh38.p12 chr11: 1,739,326-1,820,597 IFITM10, LOC105376517, 3 more genes
    nsv4527884copy number variation1nstd166human GRCh37.p13 chr11: 1,708,999-1,836,000 , GRCh38.p12 chr11: 1,687,769-1,814,770 CTSD, LOC390029, 5 more genes
    nsv4436605complex substitution1nstd102humanUncertain significance GRCh37 chr11: 870,446-1,857,751 , GRCh38.p12 chr11: 870,446-1,836,521 AP2A2, CTSD, 31 more genes
    nsv4436579complex substitution1nstd102humanUncertain significance GRCh37 chr11: 1,092,954-1,857,751 , GRCh38.p12 chr11: 1,138,209-1,836,521 CTSD, DUSP8, 24 more genes
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