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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
    nsv5279549copy number variation1nstd204human GRCh38.p13 chr11: 67,318,601-67,507,600 , GRCh37.p13 chr11: 67,086,072-67,275,071 TMEM134, PTPRCAP, 17 more genes
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    nsv5131169mobile element insertion1nstd203human GRCh38 chr11: 67,434,533-67,434,546 , GRCh37.p13 chr11: 67,202,004-67,202,017 PTPRCAP, RPS6KB2, 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
    nsv4728103copy number variation1nstd197human GRCh37 chr11: 67,203,205-67,206,420 , GRCh38.p12 chr11: 67,435,734-67,438,949 PTPRCAP, RPS6KB2, 1 more genes
    nsv4712776copy number variation1nstd195human GRCh37 chr11: 66,866,001-67,241,201 , GRCh38.p12 chr11: 67,098,530-67,473,730 PPP1CA, RPS6KB2, 19 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4455772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,081,259-67,471,729 , GRCh38.p12 chr11: 67,313,788-67,704,258 LOC100130987, RPL37P2, 27 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
    nsv3920906copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 66,741,311-68,972,547 , GRCh37 chr11: 66,984,735-69,263,366 , GRCh38 chr11: 67,217,264-69,448,598 GRK2, ALDH3B1, 82 more genes
    nsv3917536copy number variation1nstd102humanPathogenic NCBI36 chr11: 66,409,957-67,222,297 , GRCh38 chr11: 66,885,910-67,698,250 , GRCh37 chr11: 66,653,381-67,465,721 PPP1CA, TBC1D10C, 39 more genes
    nsv3913876copy number variation1nstd102humanBenign GRCh38 chr11: 67,397,196-67,644,438 , NCBI36 chr11: 66,921,243-67,168,485 , GRCh37 chr11: 67,164,667-67,411,909 RPS6KB2, GSTP1, 20 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
    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
    nsv3903195copy number variation1nstd102humanBenign GRCh37 chr11: 67,203,261-67,220,044 , GRCh38.p12 chr11: 67,435,790-67,452,573 CORO1B, RPS6KB2, 3 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
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