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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6913781copy number variation1nstd229human GRCh38 chr11: 34,168,221-36,836,658 , GRCh37.p13 chr11: 34,189,768-36,858,208 TRAF6, LOC100422241, 39 more genes
    nsv6910717copy number variation1nstd229human GRCh38 chr11: 34,456,101-34,557,300 , GRCh37.p13 chr11: 34,477,648-34,578,847 CAT, ELF5
    nsv6909314copy number variation1nstd229human GRCh38 chr11: 34,465,540-34,469,582 , GRCh37.p13 chr11: 34,487,087-34,491,129 CAT
    nsv6909164copy number variation1nstd229human GRCh38 chr11: 34,468,397-34,470,956 , GRCh37.p13 chr11: 34,489,944-34,492,503 CAT
    nsv6900371copy number variation1nstd229human GRCh38 chr11: 34,434,358-34,457,367 , GRCh37.p13 chr11: 34,455,905-34,478,914 LOC105376622, CAT
    nsv6899593copy number variation1nstd229human GRCh38 chr11: 34,452,101-34,456,700 , GRCh37.p13 chr11: 34,473,648-34,478,247 CAT
    nsv6898829copy number variation1nstd229human GRCh38 chr11: 34,433,514-34,446,062 , GRCh37.p13 chr11: 34,455,061-34,467,609 CAT, LOC105376622
    nsv6898567copy number variation1nstd229human GRCh38 chr11: 33,356,301-35,259,800 , GRCh37.p13 chr11: 33,377,847-35,281,347 C11orf91, EHF, 34 more genes
    nsv6638023copy number variation1nstd102humanPathogenic GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766 THEM7P, LOC105376624, 92 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
    nsv5914569copy number variation1nstd209human GRCh38 chr11: 34,443,162-34,444,651 , GRCh37.p13 chr11: 34,464,709-34,466,198 CAT
    nsv5861519copy number variation1nstd209human GRCh38 chr11: 34,442,790-34,444,689 , GRCh37.p13 chr11: 34,464,337-34,466,236 CAT
    nsv5705267mobile element insertion1nstd211human GRCh38 chr11: 34,443,026-34,443,026 , GRCh37.p13 chr11: 34,464,573-34,464,573 CAT
    nsv5500626copy number variation1nstd206human GRCh38 chr11: 34,446,813-34,446,881 , GRCh37.p13 chr11: 34,468,360-34,468,428 CAT
    nsv5408220mobile element insertion1nstd206human GRCh38 chr11: 34,443,026-34,443,077 , GRCh37.p13 chr11: 34,464,573-34,464,624 CAT
    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
    nsv5131107mobile element insertion1nstd203human GRCh38 chr11: 34,468,558-34,468,572 , GRCh37.p13 chr11: 34,490,105-34,490,119 CAT
    nsv5128758mobile element insertion1nstd203human GRCh38 chr11: 34,466,767-34,466,780 , GRCh37.p13 chr11: 34,488,314-34,488,327 CAT
    nsv4984386copy number variation1nstd200human GRCh38 chr11: 34,429,995-34,437,111 , GRCh37.p13 chr11: 34,451,542-34,458,658 CAT, CIR1P3, 1 more genes
    nsv4984384copy number variation1nstd200human GRCh38 chr11: 34,229,583-34,594,668 , GRCh37.p13 chr11: 34,251,130-34,616,215 CAT, ELF5, 5 more genes
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