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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
    nsv6902830copy number variation1nstd229human GRCh38 chr11: 70,097,626-70,476,174 , GRCh37.p13 chr11: 69,943,732-70,301,892 LOC107984346, LOC101928473, 8 more genes
    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
    nsv5711985mobile element insertion2nstd211human GRCh38 chr11: 70,204,005-70,204,005 , GRCh37.p13 chr11: 70,050,111-70,050,111 FADD
    nsv5399705mobile element insertion1nstd206human GRCh38 chr11: 70,204,005-70,204,056 , GRCh37.p13 chr11: 70,050,111-70,050,162 FADD
    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
    nsv5130652mobile element insertion1nstd203human GRCh38 chr11: 70,203,993-70,204,005 , GRCh37.p13 chr11: 70,050,099-70,050,111 FADD
    nsv5124130mobile element insertion1nstd203human GRCh38 chr11: 70,203,989-70,204,005 , GRCh37.p13 chr11: 70,050,095-70,050,111 FADD
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4708463copy number variation1nstd195human GRCh37 chr11: 69,774,701-70,060,251 , GRCh38.p12 chr11: 69,928,599-70,214,145 , FADD, 6 more genes
    nsv4704116copy number variation1nstd195human GRCh37 chr11: 69,774,651-70,140,751 , GRCh38.p12 chr11: 69,928,595-70,294,645 , PPFIA1, 9 more genes
    nsv4607909copy number variation1nstd183human GRCh37 chr11: 70,053,472-70,083,396 , GRCh38.p12 chr11: 70,207,366-70,237,290 FADD
    nsv4607311copy number variation1nstd183human GRCh37 chr11: 70,049,026-70,049,727 , GRCh38.p12 chr11: 70,202,920-70,203,621 FADD
    nsv4495794mobile element insertion1nstd166human GRCh37.p13 chr11: 70,050,095-70,050,095 , GRCh38.p12 chr11: 70,203,989-70,203,989 FADD
    nsv4456967copy number variation1nstd102humanUncertain significance GRCh37 chr11: 69,849,324-70,478,959 , GRCh38.p12 chr11: 70,003,218-70,632,854 H2AZP4, MIR548K, 13 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
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