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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5661386insertion1nstd207human GRCh38 chr11: 696,767-696,767 , GRCh37.p13 chr11: 696,767-696,767 TMEM80, DEAF1
    nsv5557461sequence alteration1nstd206human GRCh38 chr11: 428,013-744,860 , GRCh37.p13 chr11: 428,013-744,860 , DRD4, 21 more genes
    nsv5538558insertion1nstd206human GRCh38 chr11: 696,722-696,722 , GRCh37.p13 chr11: 696,722-696,722 DEAF1, TMEM80
    nsv5505907copy number variation1nstd206human GRCh38 chr11: 704,206-704,914 , GRCh37.p13 chr11: 704,206-704,914 DEAF1, EPS8L2, 1 more genes
    nsv5504317copy number variation1nstd206human GRCh38 chr11: 669,321-702,154 , GRCh37.p13 chr11: 669,321-702,154 TMEM80, DEAF1
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5316925copy number variation1nstd204human GRCh37.p13 chr11: 703,215-706,112 , GRCh38.p13 chr11: 703,215-706,112 DEAF1, EPS8L2, 1 more genes
    nsv5258461copy number variation1nstd204human GRCh38.p13 chr11: 520,301-974,900 , GRCh37.p13 chr11: 520,301-974,900 , SCT, 33 more genes
    nsv5256086copy number variation1nstd204human GRCh38.p13 chr11: 665,101-696,700 , GRCh37.p13 chr11: 665,101-696,700 DEAF1, TMEM80
    nsv4984100copy number variation1nstd200human GRCh38 chr11: 642,551-894,927 , GRCh37.p13 chr11: 642,551-894,927 EPS8L2, PNPLA2, 17 more genes
    nsv4977788copy number variation1nstd200human GRCh38 chr11: 695,299-695,572 , GRCh37.p13 chr11: 695,299-695,572 DEAF1, TMEM80
    nsv4836915copy number variation1nstd200human GRCh37 chr11: 642,551-894,927 , GRCh38.p12 chr11: 642,551-894,927 CHID1, PANO1, 17 more genes
    nsv4830867copy number variation1nstd200human GRCh37 chr11: 703,218-706,111 , GRCh38.p12 chr11: 703,218-706,111 DEAF1, TMEM80, 1 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4753234insertion1nstd199human GRCh37 chr11: 696,749-696,749 , GRCh38.p12 chr11: 696,749-696,749 DEAF1, TMEM80
    nsv4729665copy number variation1nstd102humanUncertain significance GRCh37 chr11: 230,615-1,150,353 , GRCh38.p12 chr11: 230,615-1,156,726 CD151, RPLP2, 57 more genes
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4682252copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-795,026 , GRCh38.p12 chr11|NT_187586.1: 62,257-209,248 , GRCh38.p12 chr11: 532,616-795,026 LMNTD2, LRRC56, 20 more genes
    nsv4681827copy number variation1nstd102humanUncertain significance GRCh37 chr11: 532,616-2,906,985 , GRCh38.p12 chr11: 532,616-2,885,755 LOC105376517, KRTAP5-2, 99 more genes
    nsv4681514copy number variation2nstd102humanUncertain significance GRCh37 chr11: 612,625-2,193,840 , GRCh38.p12 chr11: 612,625-2,172,610 LINC02688, TNNI2, 74 more genes
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