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Items: 1 to 20 of 108

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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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5198700mobile element insertion1nstd203human GRCh38 chr11: 47,446,084-47,446,100 , GRCh37.p13 chr11: 47,467,636-47,467,652 RAPSN
    nsv5131650mobile element insertion1nstd203human GRCh38 chr11: 47,443,931-47,443,959 , GRCh37.p13 chr11: 47,465,483-47,465,511 RAPSN
    nsv5123695mobile element insertion1nstd203human GRCh38 chr11: 47,445,068-47,445,073 , GRCh37.p13 chr11: 47,466,620-47,466,625 RAPSN
    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
    nsv4682636copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,469,354-47,470,727 , GRCh38.p12 chr11: 47,447,802-47,449,175 RAPSN
    nsv4681027copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,459,516-47,460,492 , GRCh38.p12 chr11: 47,437,965-47,438,941 RAPSN
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3914709copy number variation1nstd102humanPathogenic GRCh38 chr11: 46,840,454-48,643,003 , GRCh37 chr11: 46,862,005-48,664,555 , NCBI36 chr11: 46,818,581-48,621,131 CELF1, C1QTNF4, 56 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 ACP2, ARHGAP1, 143 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 MIR3160-1, RPS20P26, 162 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
    nsv3878248copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,459,506-47,460,502 , GRCh38 chr11: 47,437,955-47,438,951 RAPSN
    nsv3871318copy number variation1nstd102humanPathogenic GRCh37 chr11: 46,880,514-47,470,726 , GRCh38.p12 chr11: 46,858,963-47,449,174 LOC112268075, NR1H3, 17 more genes
    nsv3244955insertion9nstd152human GRCh38 chr11: 47,428,566-47,438,836 , GRCh37.p13 chr11: 47,450,117-47,460,387 RAPSN
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
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