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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    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
    nsv5263198copy number variation1nstd204human GRCh38.p13 chr11: 57,038,501-57,043,900 , GRCh37.p13 chr11: 56,805,976-56,811,375 OR5AK4P, OR5AO1P, 1 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
    nsv4680588copy number variation1nstd189human GRCh37.p13 chr11: 55,444,212-57,222,540 , GRCh38.p12 chr11: 55,676,736-57,455,067 , APLNR, 109 more genes
    nsv4453292copy number variation1nstd102humannot provided GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254 OR8J3, LINC02735, 150 more genes
    nsv4384042copy number variation1nstd173human GRCh37 chr11: 55,212,270-56,906,448 , GRCh38.p12 chr11: 55,444,794-57,138,974 OR5BQ1P, OR5AL1, 111 more genes
    nsv4376896copy number variation1nstd173human GRCh37 chr11: 55,212,275-56,906,448 , GRCh38.p12 chr11: 55,444,799-57,138,974 OR5BP1P, FAM8A2P, 111 more genes
    nsv4211935copy number variation1nstd166human GRCh37.p13 chr11: 56,677,904-56,832,293 , GRCh38.p12 chr11: 56,910,428-57,064,818 OR5BQ1P, OR5BP1P, 7 more genes
    nsv3924646copy number variation1nstd102humanUncertain significance GRCh38 chr11: 55,316,535-57,539,457 , GRCh37 chr11: 55,084,011-57,306,930 , NCBI36 chr11: 54,840,587-57,063,506 OR5AL1, OR5AK2, 134 more genes
    nsv3924455copy number variation1nstd102humanBenign GRCh38 chr11: 55,445,689-57,114,783 , GRCh37 chr11: 55,213,165-56,882,257 , NCBI36 chr11: 54,969,741-56,638,833 OR5AL1, OR5F2P, 111 more genes
    nsv3918615copy number variation1nstd102humanUncertain significance NCBI36 chr11: 54,789,872-56,896,303 , GRCh37.p13 chr11: 55,033,296-57,139,727 , GRCh38.p12 chr11: 55,265,820-57,372,254 OR8K5, OR5G5P, 127 more genes
    nsv3911150copy number variation1nstd102humanPathogenic GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777 OR5BD1P, SELENOH, 197 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
    nsv3904152copy number variation1nstd102humanUncertain significance GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953 FAM111B, OR5M1, 250 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
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