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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5557461sequence alteration1nstd206human GRCh38 chr11: 428,013-744,860 , GRCh37.p13 chr11: 428,013-744,860 , DRD4, 21 more genes
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5258461copy number variation1nstd204human GRCh38.p13 chr11: 520,301-974,900 , GRCh37.p13 chr11: 520,301-974,900 , SCT, 33 more genes
    nsv5248917copy number variation1nstd204human GRCh38.p13 chr11: 322,701-664,500 , GRCh37.p13 chr11: 322,701-664,500 , ANO9, 23 more genes
    nsv4984099copy number variation1nstd200human GRCh38 chr11: 610,120-632,005 , GRCh37.p13 chr11: 610,120-632,005 SCT, PHRF1, 2 more genes
    nsv4977777copy number variation1nstd200human GRCh38 chr11: 622,619-630,791 , GRCh37.p13 chr11: 622,619-630,791 SCT, CDHR5
    nsv4977776copy number variation1nstd200human GRCh38 chr11: 620,595-625,866 , GRCh37.p13 chr11: 620,595-625,866 SCT, CDHR5
    nsv4831817copy number variation1nstd200human GRCh37 chr11: 610,120-632,005 , GRCh38.p12 chr11|NT_187586.1: 140,013-161,878 , GRCh38.p12 chr11: 610,120-632,005 PHRF1, SCT, 2 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
    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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4673760copy number variation1nstd186human GRCh37 chr11: 625,001-628,000 , GRCh38.p12 chr11: 625,001-628,000 , GRCh38.p12 chr11|NT_187586.1: 154,900-157,899 SCT, CDHR5
    nsv4610883copy number variation1nstd183human GRCh37 chr11: 626,970-627,431 , GRCh38.p12 chr11: 626,970-627,431 , GRCh38.p12 chr11|NT_187586.1: 156,869-157,330 SCT
    nsv4602878copy number variation1nstd183human GRCh37 chr11: 625,001-628,000 , GRCh38.p12 chr11: 625,001-628,000 , GRCh38.p12 chr11|NT_187586.1: 154,900-157,899 SCT, CDHR5
    nsv4599591copy number variation1nstd183human GRCh37 chr11: 350,509-943,372 , GRCh38.p12 chr11: 350,509-943,372 , B4GALNT4, 40 more genes
    nsv4599096copy number variation1nstd183human GRCh37 chr11: 482,149-692,445 , GRCh38.p12 chr11: 482,149-692,445 , GRCh38.p12 chr11|NT_187586.1: 11,790-209,248 , PHRF1, 16 more genes
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