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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5660209insertion1nstd207human GRCh38 chr11: 822,208-822,208 , GRCh37.p13 chr11: 822,208-822,208 PNPLA2
    nsv5380885copy number variation1nstd102humanUncertain significance GRCh37 chr11: 298,501-4,113,028 , GRCh38.p12 chr11: 298,501-4,091,798 LINC02688, MIR210, 156 more genes
    nsv5317479copy number variation1nstd204human GRCh38.p13 chr11: 708,633-1,150,137 , GRCh37.p13 chr11: 708,633-1,144,045 MUC2, CRACR2B, 21 more genes
    nsv5258461copy number variation1nstd204human GRCh38.p13 chr11: 520,301-974,900 , GRCh37.p13 chr11: 520,301-974,900 , SCT, 33 more genes
    nsv5242369copy number variation1nstd204human GRCh37.p13 chr11: 800,301-881,400 , GRCh38.p13 chr11: 800,301-881,400 CD151, POLR2L, 7 more genes
    nsv4984101copy number variation1nstd200human GRCh38 chr11: 708,641-1,150,129 , GRCh37.p13 chr11: 708,641-1,144,037 POLR2L, MUC6, 21 more genes
    nsv4984100copy number variation1nstd200human GRCh38 chr11: 642,551-894,927 , GRCh37.p13 chr11: 642,551-894,927 EPS8L2, PNPLA2, 17 more genes
    nsv4977796copy number variation1nstd200human GRCh38 chr11: 814,509-817,177 , GRCh37.p13 chr11: 814,509-817,177 PNPLA2
    nsv4843772copy number variation1nstd200human GRCh37 chr11: 708,641-1,144,037 , GRCh38.p12 chr11|NT_187681.1: 1-218,430 , GRCh38.p12 chr11: 708,641-1,150,129 SLC25A22, PANO1, 21 more genes
    nsv4836915copy number variation1nstd200human GRCh37 chr11: 642,551-894,927 , GRCh38.p12 chr11: 642,551-894,927 CHID1, PANO1, 17 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
    nsv4682259copy number variation1nstd102humanUncertain significance GRCh37 chr11: 819,709-824,872 , GRCh38.p12 chr11: 819,709-824,872 PNPLA2, CRACR2B
    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
    nsv4612327copy number variation1nstd183human GRCh37 chr11: 772,982-933,581 , GRCh38.p12 chr11: 772,982-933,581 PNPLA2, CD151, 13 more genes
    nsv4599591copy number variation1nstd183human GRCh37 chr11: 350,509-943,372 , GRCh38.p12 chr11: 350,509-943,372 , B4GALNT4, 40 more genes
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