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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv6911326copy number variation1nstd229human GRCh38 chr11: 69,696,701-69,783,000 , GRCh37.p13 chr11: 69,511,469-69,597,768 FGF19, DNAJB6P5, 1 more genes
    nsv6904338copy number variation1nstd229human GRCh38 chr11: 69,155,401-69,991,100 , GRCh37.p13 chr11: 68,922,869-69,614,785 LOC338694, LOC105369370, 17 more genes
    nsv6900732copy number variation1nstd229human GRCh38 chr11: 69,588,671-70,124,332 , GRCh37.p13 chr11|NW_003571046.1: 1-276,448 , GRCh37.p13 chr11: 69,403,439-69,970,438 FGF19, LOC105369371, 10 more genes
    nsv6900504copy number variation1nstd229human GRCh38 chr11: 69,768,948-69,769,299 , GRCh37.p13 chr11: 69,583,716-69,584,067 FGF4
    nsv6637600copy number variation1nstd102humanUncertain significance GRCh37 chr11: 69,559,588-70,347,818 , GRCh38.p12 chr11: 69,744,820-70,501,713 LOC107984368, ANO1, 15 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6290813copy number variation1nstd102humanPathogenic GRCh37 chr11: 69,214,835-70,821,137 , GRCh38.p12 chr11: 69,400,067-71,110,091 CCND1, LOC101928473, 25 more genes
    nsv5502305copy number variation1nstd206human GRCh38 chr11: 69,766,592-69,771,818 , GRCh37.p13 chr11: 69,581,360-69,586,586 FGF4
    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
    nsv5278908copy number variation1nstd204human GRCh38.p13 chr11: 69,768,398-69,782,762 , GRCh37.p13 chr11: 69,583,166-69,597,530 FGF4
    nsv5270994copy number variation1nstd204human GRCh38.p13 chr11: 69,761,701-69,790,300 , GRCh37.p13 chr11: 69,576,469-69,605,068 FGF4
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4710825copy number variation1nstd195human GRCh37 chr11: 69,409,751-69,724,701 , GRCh38.p12 chr11: 69,594,983-69,909,959 CCND1, FGF3, 5 more genes
    nsv4706518copy number variation1nstd195human GRCh37 chr11: 69,139,801-69,724,701 , GRCh38.p12 chr11: 69,325,035-69,909,959 FGF3, LOC107984368, 9 more genes
    nsv4456202copy number variation1nstd102humanUncertain significance GRCh37 chr11: 69,540,125-69,711,472 , GRCh38.p12 chr11: 69,725,357-69,896,705 FGF3, FGF4, 2 more genes
    nsv3917463copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 67,555,736-70,982,189 , GRCh37 chr11: 67,799,160-71,304,541 , GRCh38 chr11: 68,031,693-71,593,495 CCND1, CHKA, 71 more genes
    nsv3909768copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 67,799,160-70,701,268 , GRCh38.p12 chr11: 68,031,693-70,855,163 CCND1, CHKA, 56 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
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