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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
    nsv5355294translocation1nstd200human GRCh38 chr11: 65,781,441-65,781,441 , GRCh38 chr11: 65,781,518-65,781,518 , GRCh37.p13 chr11: 65,548,989-65,548,989 , GRCh37.p13 chr11: 65,548,912-65,548,912 AP5B1
    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
    nsv4979852copy number variation1nstd200human GRCh38 chr11: 65,769,230-65,773,700 , GRCh37.p13 chr11: 65,536,701-65,541,171 AP5B1
    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
    nsv4729345copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,514,044-65,571,198 , GRCh38.p12 chr11: 65,746,573-65,803,727 OVOL1-AS1, AP5B1, 1 more genes
    nsv4457151copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,529,506-65,649,002 , GRCh38.p12 chr11: 65,762,035-65,881,531 MUS81, CTSW, 6 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
    nsv4200150copy number variation1nstd166human GRCh37.p13 chr11: 65,545,986-65,546,045 , GRCh38.p12 chr11: 65,778,515-65,778,574 AP5B1
    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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 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
    nsv2786842copy number variation1nstd132human NCBI36 chr11: 64,726,235-65,484,375 , GRCh37.p13 chr11: 64,969,659-65,727,799 , GRCh38.p12 chr11: 65,202,188-65,960,328 , MAP3K11, 51 more genes
    nsv1591543short tandem repeat2nstd128human GRCh37 chr11: 65,541,299-65,541,317 , GRCh38.p12 chr11: 65,773,828-65,773,846 AP5B1
    nsv1590876short tandem repeat1nstd128human GRCh37 chr11: 65,543,364-65,543,379 , GRCh38.p12 chr11: 65,775,893-65,775,908 AP5B1
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