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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063337inversion1nstd229human GRCh38 chr11: 6,102,736-6,119,208 , GRCh37.p13 chr11: 6,123,966-6,140,438 OR56B4
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6916735copy number variation1nstd229human GRCh38 chr11: 6,018,863-6,116,684 , GRCh37.p13 chr11: 6,040,093-6,137,914 OR56B4, OR56A7P, 4 more genes
    nsv6904589copy number variation1nstd229human GRCh38 chr11: 6,107,420-6,113,190 , GRCh37.p13 chr11: 6,128,650-6,134,420 OR56B4
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6621257copy number variation1nstd224human GRCh37 chr11: 6,041,247-6,129,756 , GRCh38.p12 chr11: 6,020,017-6,108,526 OR52X1P, OR52L2P, 4 more genes
    nsv6451818copy number variation1nstd223human GRCh38 chr11: 6,018,863-6,116,688 , GRCh37.p13 chr11: 6,040,093-6,137,918 OR56A1, OR56A7P, 4 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6247721mobile element insertion1nstd215human GRCh38 chr11: 6,106,637-6,106,637 , GRCh37.p13 chr11: 6,127,867-6,127,867 OR56B4
    nsv5125045mobile element insertion1nstd203human GRCh38 chr11: 6,106,258-6,106,272 , GRCh37.p13 chr11: 6,127,488-6,127,502 OR56B4
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 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
    nsv4681173copy number variation2nstd102humanUncertain significance GRCh37 chr11: 5,709,028-6,640,651 , GRCh38.p12 chr11: 5,687,798-6,619,420 OR56B2P, TRIM3, 50 more genes
    nsv4675693copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,505,304-6,199,376 , GRCh38.p12 chr11: 5,484,074-6,178,146 OR52B5P, HNRNPA1P53, 47 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
    nsv4603739copy number variation2nstd183human GRCh37 chr11: 6,005,905-6,159,840 , GRCh38.p12 chr11: 5,984,675-6,138,610 OR56A4, OR56A1, 9 more genes
    nsv4573189sequence alteration1nstd166human GRCh37.p13 chr11: 6,120,951-6,140,439 , GRCh38.p12 chr11: 6,099,721-6,119,209 OR56B4
    nsv4456235copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,896,551-6,719,852 , GRCh38.p12 chr11: 5,875,321-6,698,621 OR52X1P, LOC112268071, 40 more genes
    nsv4387795copy number variation1nstd173human GRCh37 chr11: 5,067,391-6,257,231 , GRCh38.p12 chr11: 5,046,161-6,236,001 HBD, OR52N2, 85 more genes
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