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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
    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
    nsv4456974copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,487,052-62,788,240 , GRCh38.p12 chr11: 62,719,580-63,020,768 RN7SL259P, SNORD29, 29 more genes
    nsv4455787copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,314,663-62,788,240 , GRCh38.p12 chr11: 62,547,191-63,020,768 TTC9C, POLR2G, 48 more genes
    nsv3924003copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 62,417,274-63,859,091 , GRCh37 chr11: 62,660,698-64,102,515 , GRCh38 chr11: 62,893,226-64,335,043 BAD, CCND2P1, 58 more genes
    nsv3922416copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,433,886-63,096,003 , NCBI36 chr11: 61,957,934-62,620,051 , GRCh37 chr11: 62,201,358-62,863,475 TAF6L, TMEM179B, 51 more genes
    nsv3912559copy number variation1nstd102humanPathogenic GRCh38 chr11: 62,249,520-62,946,093 , GRCh37 chr11: 62,016,992-62,713,565 , NCBI36 chr11: 61,773,568-62,470,141 SNORD28, SCGB1A1, 53 more genes
    nsv3909634copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 61,840,997-62,987,330 , GRCh38.p12 chr11: 62,073,525-63,219,858 CHRM1, EEF1G, 66 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
    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
    nsv3146447copy number variation1nstd151human GRCh37 chr11: 62,530,336-62,782,435 , GRCh38.p12 chr11: 62,762,864-63,014,963 SNORD22, STX5, 25 more genes
    nsv1589682short tandem repeat1nstd128human GRCh37 chr11: 62,689,775-62,689,796 , GRCh38.p12 chr11: 62,922,303-62,922,324 LOC105369333, CHRM1
    nsv1589680short tandem repeat2nstd128human GRCh37 chr11: 62,681,410-62,681,430 , GRCh38.p12 chr11: 62,913,938-62,913,958 CHRM1, LOC105369333
    nsv1589075short tandem repeat2nstd128human GRCh37 chr11: 62,681,323-62,681,334 , GRCh38.p12 chr11: 62,913,851-62,913,862 CHRM1, LOC105369333
    nsv1588337short tandem repeat1nstd128human GRCh37 chr11: 62,689,281-62,689,300 , GRCh38.p12 chr11: 62,921,809-62,921,828 LOC105369333, CHRM1
    nsv1588336short tandem repeat5nstd128human GRCh37 chr11: 62,681,144-62,681,165 , GRCh38.p12 chr11: 62,913,672-62,913,693 CHRM1, LOC105369333
    nsv1587223short tandem repeat1nstd128human GRCh37 chr11: 62,683,269-62,683,297 , GRCh38.p12 chr11: 62,915,797-62,915,825 LOC105369333, CHRM1
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