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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978805insertion1nstd209human GRCh38 chr11: 65,567,803-65,567,803 , GRCh37.p13 chr11: 65,335,274-65,335,274 ZNRD2-DT
    nsv5730646mobile element insertion2nstd211human GRCh38 chr11: 65,567,838-65,567,838 , GRCh37.p13 chr11: 65,335,309-65,335,309 ZNRD2-DT
    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
    nsv5272481copy number variation1nstd204human GRCh38.p13 chr11: 65,533,701-65,718,000 , GRCh37.p13 chr11: 65,301,172-65,485,471 ZNRD2, ZNRD2-DT, 15 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5262374copy number variation1nstd204human GRCh38.p13 chr11: 65,373,701-65,675,900 , GRCh37.p13 chr11: 65,141,172-65,443,371 , MIR612, 23 more genes
    nsv5196215mobile element insertion1nstd203human GRCh38 chr11: 65,567,823-65,567,838 , GRCh37.p13 chr11: 65,335,294-65,335,309 ZNRD2-DT
    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
    nsv4615174copy number variation1nstd183human GRCh37 chr11: 65,153,786-65,437,098 , GRCh38.p12 chr11: 65,386,315-65,669,627 , RELA, 22 more genes
    nsv4613170copy number variation1nstd183human GRCh37 chr11: 65,321,280-65,341,671 , GRCh38.p12 chr11: 65,553,809-65,574,200 ZNRD2, FAM89B, 3 more genes
    nsv4607743copy number variation1nstd183human GRCh37 chr11: 65,257,456-65,362,478 , GRCh38.p12 chr11: 65,489,985-65,595,007 EHBP1L1, KCNK7, 10 more genes
    nsv4575847mobile element insertion1nstd166human GRCh37.p13 chr11: 65,335,294-65,335,294 , GRCh38.p12 chr11: 65,567,823-65,567,823 ZNRD2-DT
    nsv4436237copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205 ARL2, BAD, 117 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv3920374copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,288,302-65,462,820 , GRCh38 chr11: 65,520,831-65,695,349 , NCBI36 chr11: 65,044,878-65,219,396 ZNRD2, ZNRD2-DT, 13 more genes
    nsv3913578copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,095,257-65,393,902 , GRCh38 chr11: 65,327,786-65,626,431 , NCBI36 chr11: 64,851,833-65,150,478 KCNK7, LINC02736, 19 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
    nsv3902272copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787 ACTN3, GRK2, 157 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
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