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Items: 1 to 20 of 99

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    nsv7069956inversion1nstd229human GRCh38 chr11: 5,352,767-5,352,846 , GRCh37.p13 chr11: 5,373,997-5,374,076 OR51B6, LOC100418885, 1 more genes
    nsv7063495inversion1nstd229human GRCh38 chr11: 5,016,392-5,387,994 , GRCh37.p13 chr11: 5,037,622-5,409,224 OR51M1, OR52J2P, 29 more genes
    nsv7060711inversion1nstd229human GRCh38 chr11: 5,052,261-5,434,559 , GRCh37.p13 chr11: 5,073,491-5,455,789 HBD, OR52S1P, 29 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
    nsv6913749copy number variation1nstd229human GRCh38 chr11: 5,339,887-5,351,118 , GRCh37.p13 chr11: 5,361,117-5,372,348 OR51B6, OR51B5
    nsv6638042copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,361,272-5,660,023 , GRCh38.p12 chr11: 5,340,042-5,638,793 OR51A10P, OR52H2P, 24 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
    nsv6637234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 5,279,153-5,619,949 , GRCh38.p12 chr11: 5,257,923-5,598,719 OR51A10P, OR51B5, 29 more genes
    nsv6621246copy number variation1nstd224human GRCh37 chr11: 5,372,751-5,444,353 , GRCh38.p12 chr11: 5,351,521-5,423,123 OR51J1, OR51B5, 5 more genes
    nsv6449237copy number variation1nstd223human GRCh38 chr11: 5,339,879-5,351,114 , GRCh37.p13 chr11: 5,361,109-5,372,344 OR51B6, OR51B5
    nsv6448416copy number variation1nstd223human GRCh38 chr11: 5,315,096-5,363,305 , GRCh37.p13 chr11: 5,336,326-5,384,535 OR51B6, OR51B8P, 5 more genes
    nsv6445670copy number variation1nstd223human GRCh38 chr11: 5,348,692-5,349,897 , GRCh37.p13 chr11: 5,369,922-5,371,127 OR51B5, OR51B6
    nsv6436221copy number variation1nstd223human GRCh38 chr11: 5,301,605-5,397,946 , GRCh37.p13 chr11: 5,322,835-5,419,176 OR51B4, OR51B3P, 7 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
    nsv6291427copy number variation1nstd102humannot provided GRCh37 chr11: 230,615-5,525,355 , GRCh38.p12 chr11: 230,615-5,504,125 OR52J1P, IFITM1, 255 more genes
    nsv6290806copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,373,646-5,519,671 , GRCh38.p12 chr11: 5,352,416-5,498,441 OR51Q1, OR51B6, 10 more genes
    nsv4978005copy number variation1nstd200human GRCh38 chr11: 5,351,084-5,363,532 , GRCh37.p13 chr11: 5,372,314-5,384,762 TMEM258P1, LOC100418885, 2 more genes
    nsv4978004copy number variation1nstd200human GRCh38 chr11: 5,350,419-5,351,857 , GRCh37.p13 chr11: 5,371,649-5,373,087 OR51B5, OR51B6
    nsv4978002copy number variation1nstd200human GRCh38 chr11: 5,339,877-5,351,114 , GRCh37.p13 chr11: 5,361,107-5,372,344 OR51B6, OR51B5
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