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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 ACY3, FAUP4, 2031 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 ACY3, MIR6860, 106 more genes
    nsv3915534copy number variation1nstd102humanPathogenic NCBI36 chr11: 66,970,200-68,203,117 , GRCh38 chr11: 67,446,153-68,679,073 , GRCh37 chr11: 67,213,624-68,446,541 ACY3, LOC107984343, 46 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 ACY3, PPP1CA, 39 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 ACY3, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 ACY3, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 ACY3, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 ACY3, PYGM, 2125 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 ACY3, SNORD13F, 141 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 ACY3, B4GAT1, 90 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 ACY3, GRK2, 82 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 ACY3, RPS6KB2, 20 more genes
    nsv3907435copy number variation1nstd102humanBenign GRCh37 chr11: 67,349,872-67,715,028 , GRCh38.p12 chr11: 67,582,401-67,947,557 ACY3, LOC105369359, 21 more genes
    nsv3896688copy number variation1nstd102humanBenign GRCh37 chr11: 67,331,526-67,693,404 , GRCh38.p12 chr11: 67,564,055-67,925,933 ACY3, GSTP1, 20 more genes
    nsv3918462copy number variation1nstd102humanUncertain significance NCBI36 chr11: 67,114,780-67,222,297 , GRCh38 chr11: 67,590,733-67,698,250 , GRCh37 chr11: 67,358,204-67,465,721 ACY3, DOC2GP, 6 more genes
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 ACY3, B4GAT1, 208 more genes
    nsv3904873copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,024,774-67,430,781 , GRCh38.p12 chr11: 66,257,303-67,663,310 ACY3, B4GAT1-DT, 79 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 ACY3, PPP1CA, 58 more genes
    nsv4455772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,081,259-67,471,729 , GRCh38.p12 chr11: 67,313,788-67,704,258 ACY3, LOC100130987, 27 more genes
    nsv3922289copy number variation1nstd102humanUncertain significance GRCh38 chr11: 67,590,733-67,806,931 , NCBI36 chr11: 67,114,780-67,330,978 , GRCh37 chr11: 67,358,204-67,574,402 ACY3, NDUFV1-DT, 13 more genes
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