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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
    nsv5268498copy number variation1nstd204human GRCh38.p13 chr11: 62,450,801-62,721,600 , GRCh37.p13 chr11: 62,218,273-62,489,072 HNRNPUL2-BSCL2, GANAB, 19 more genes
    nsv4979702copy number variation1nstd200human GRCh38 chr11: 62,563,057-62,565,026 , GRCh37.p13 chr11: 62,330,529-62,332,498 MIR6747, EEF1G
    nsv4839544copy number variation1nstd200human GRCh37 chr11: 62,330,530-62,332,498 , GRCh38.p12 chr11: 62,563,058-62,565,026 MIR6747, EEF1G
    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
    nsv4675148copy number variation1nstd102humanUncertain significance GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806 LOC105369326, MS4A18, 91 more genes
    nsv4570455sequence alteration1nstd166human GRCh37.p13 chr11: 62,194,945-62,500,073 , GRCh38.p12 chr11: 62,427,473-62,732,601 MTA2, GANAB, 21 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
    nsv4424656copy number variation1nstd174human GRCh37 chr11: 62,262,742-62,410,577 , GRCh38.p12 chr11: 62,495,270-62,643,105 EEF1G, ROM1, 7 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
    nsv3913554copy number variation1nstd102humanPathogenic NCBI36 chr11: 61,976,619-62,386,829 , GRCh37 chr11: 62,220,043-62,630,253 , GRCh38 chr11: 62,452,571-62,862,781 NXF1, SNORA57, 43 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
    nsv3911700copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,330,308-62,608,042 , GRCh38 chr11: 62,562,836-62,840,570 , NCBI36 chr11: 62,086,884-62,364,618 TAF6L, CSKMT, 32 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
    nsv3901327copy number variation1nstd102humanBenign GRCh37 chr11: 62,157,418-62,362,465 , GRCh38.p12 chr11: 62,389,946-62,594,993 MTA2, TUT1, 6 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
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