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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5502001copy number variation1nstd206human GRCh38 chr11: 65,651,926-65,652,012 , GRCh37.p13 chr11: 65,419,397-65,419,483 RELA
    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
    nsv5277971copy number variation1nstd204human GRCh38.p13 chr11: 65,652,918-65,653,917 , GRCh37.p13 chr11: 65,420,389-65,421,388 RELA
    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
    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
    nsv4609446copy number variation1nstd183human GRCh37 chr11: 65,429,580-65,430,400 , GRCh38.p12 chr11: 65,662,109-65,662,929 RELA-DT, RELA
    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
    nsv4207786copy number variation1nstd166human GRCh37.p13 chr11: 65,422,475-65,423,158 , GRCh38.p12 chr11: 65,655,004-65,655,687 RELA
    nsv4204103copy number variation1nstd166human GRCh37.p13 chr11: 65,425,972-65,426,188 , GRCh38.p12 chr11: 65,658,501-65,658,717 RELA
    nsv3956503copy number variation1nstd168human GRCh38 chr11: 65,659,783-65,698,908 , GRCh37.p13 chr11: 65,427,254-65,466,379 RELA, RELA-DT, 1 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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3903507copy number variation1nstd102humanBenign GRCh37 chr11: 65,347,930-65,421,892 , GRCh38.p12 chr11: 65,580,459-65,654,421 MIR4690, EHBP1L1, 6 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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