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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147437copy number variation1nstd232human GRCh37.p13 chr11: 6,630,870-6,630,953 , GRCh38.p12 chr11: 6,609,639-6,609,722 ILK, TAF10
    nsv7144298copy number variation1nstd232human GRCh37.p13 chr11: 6,630,637-6,630,739 , GRCh38.p12 chr11: 6,609,406-6,609,508 ILK, TAF10
    nsv7138606copy number variation1nstd232human GRCh37.p13 chr11: 6,630,018-6,630,111 , GRCh38.p12 chr11: 6,608,788-6,608,880 ILK, TAF10
    nsv7094097copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,625,502-6,662,844 , GRCh38.p12 chr11: 6,604,272-6,641,613 TPP1, ILK, 2 more genes
    nsv7093698copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,411,829-6,662,844 , GRCh38.p12 chr11: 6,390,599-6,641,613 SMPD1, HPX, 11 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6914096copy number variation1nstd229human GRCh38 chr11: 6,602,038-6,603,266 , GRCh37.p13 chr11: 6,623,268-6,624,496 RRP8, ILK
    nsv6907285copy number variation1nstd229human GRCh38 chr11: 6,603,909-6,606,784 , GRCh37.p13 chr11: 6,625,139-6,628,014 ILK, RRP8, 1 more genes
    nsv6905815copy number variation1nstd229human GRCh38 chr11: 6,608,101-6,615,600 , GRCh37.p13 chr11: 6,629,331-6,636,831 TPP1, ILK, 1 more genes
    nsv6905729copy number variation1nstd229human GRCh38 chr11: 6,595,782-6,605,207 , GRCh37.p13 chr11: 6,617,012-6,626,437 TAF10, RRP8, 1 more genes
    nsv6903104copy number variation1nstd229human GRCh38 chr11: 6,545,701-6,661,700 , GRCh37.p13 chr11: 6,566,931-6,682,931 TPP1, DNHD1, 4 more genes
    nsv6899514copy number variation1nstd229human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 RRP8, OR2AG1, 19 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6454569copy number variation1nstd223human GRCh38 chr11: 6,603,909-6,606,779 , GRCh37.p13 chr11: 6,625,139-6,628,009 ILK, TAF10, 1 more genes
    nsv6437234copy number variation1nstd223human GRCh38 chr11: 6,602,704-6,989,609 , GRCh37.p13 chr11: 6,623,934-7,010,840 ILK, OR2D2, 19 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6290772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,502,523-7,248,333 , GRCh38.p12 chr11: 6,481,293-7,227,102 GVINP2, OR2AG2, 26 more genes
    nsv6132268copy number variation1nstd213human GRCh37 chr11: 6,320,000-6,880,001 , GRCh38.p12 chr11: 6,298,770-6,858,770 APBB1, TPP1, 22 more genes
    nsv5699620mobile element insertion2nstd211human GRCh38 chr11: 6,602,361-6,602,361 , GRCh37.p13 chr11: 6,623,591-6,623,591 ILK, RRP8
    nsv5672634copy number variation1nstd102humanPathogenic GRCh37 chr11: 6,559,613-6,640,631 , GRCh38.p12 chr11: 6,538,383-6,619,400 TPP1, ILK, 4 more genes
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