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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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 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
    nsv4453555copy number variation1nstd102humanUncertain significance GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026 CNIH2, YIF1A, 33 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv3921639copy number variation1nstd102humanPathogenic NCBI36 chr11: 65,265,478-67,229,716 , GRCh37 chr11: 65,508,902-67,473,140 , GRCh38 chr11: 65,741,431-67,705,669 MIR6860, DOC2GP, 106 more genes
    nsv3911732copy number variation1nstd102humanPathogenic GRCh38 chr11: 66,193,502-67,890,770 , GRCh37 chr11: 65,960,973-67,658,241 , NCBI36 chr11: 65,717,549-67,414,817 B4GAT1, KDM2A, 90 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
    nsv3905271copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,906,060-66,086,140 , GRCh38.p12 chr11: 66,138,589-66,318,669 KLC2-AS1, TMEM151A, 9 more genes
    nsv3904873copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,024,774-67,430,781 , GRCh38.p12 chr11: 66,257,303-67,663,310 B4GAT1-DT, RNU7-23P, 79 more genes
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 ACTN3, GRK2, 157 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
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3167936inversion1nstd158human GRCh37 chr11: 64,590,560-68,196,411 , GRCh38.p12 chr11: 64,823,088-68,428,943 , ACTN3, 210 more genes
    nsv3153589copy number variation1nstd151human GRCh37 chr11: 66,031,128-66,039,728 , GRCh38.p12 chr11: 66,263,657-66,272,257 KLC2-AS2, RAB1B, 3 more genes
    nsv2782860copy number variation1nstd132human NCBI36 chr11: 65,746,334-66,316,599 , GRCh37.p13 chr11: 65,989,758-66,560,023 , GRCh38.p12 chr11: 66,222,287-66,792,552 SPTBN2, PACS1, 38 more genes
    nsv2753065copy number variation1nstd130human GRCh37 chr11: 66,031,402-66,066,349 , GRCh38.p12 chr11: 66,263,931-66,298,878 KLC2, CNIH2, 6 more genes
    nsv1592335short tandem repeat1nstd128human GRCh37 chr11: 66,036,136-66,036,150 , GRCh38.p12 chr11: 66,268,665-66,268,679 RAB1B, KLC2-AS2
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