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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
    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
    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
    nsv3918477copy number variation1nstd102humanUncertain significance GRCh38 chr11: 57,372,226-57,936,167 , NCBI36 chr11: 56,896,275-57,460,215 , GRCh37 chr11: 57,139,699-57,703,639 TMX2-CTNND1, CTNND1, 26 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
    nsv3900116copy number variation1nstd102humanUncertain significance GRCh37 chr11: 57,182,779-57,244,361 , GRCh38.p12 chr11: 57,415,306-57,476,888 RN7SKP259, SLC43A3, 2 more genes
    nsv3899876copy number variation1nstd102humanBenign GRCh37 chr11: 57,147,016-57,667,222 , GRCh38.p12 chr11: 57,379,543-57,899,750 PRG3, UBE2L6, 24 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
    nsv3150131copy number variation1nstd151human GRCh37 chr11: 57,157,357-57,175,374 , GRCh38.p12 chr11: 57,389,884-57,407,901 , PRG2, 1 more genes
    nsv3147235copy number variation1nstd151human GRCh37 chr11: 57,075,866-57,184,148 , GRCh38.p12 chr11: 57,308,392-57,416,675 , SLC43A3, 5 more genes
    nsv1586607short tandem repeat1nstd128human GRCh37 chr11: 57,183,236-57,183,252 , GRCh38.p12 chr11: 57,415,763-57,415,779 SLC43A3
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