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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979044insertion1nstd209human GRCh38 chr11: 66,615,753-66,615,753 , GRCh37.p13 chr11: 66,383,224-66,383,224 RBM14, RBM14-RBM4
    nsv5709536mobile element insertion1nstd211human GRCh38 chr11: 66,626,058-66,626,058 , GRCh37.p13 chr11: 66,393,529-66,393,529 RBM14-RBM4, RBM14
    nsv5662700insertion1nstd207human GRCh38 chr11: 66,615,753-66,615,753 , GRCh37.p13 chr11: 66,383,224-66,383,224 RBM14-RBM4, RBM14
    nsv5547304insertion1nstd206human GRCh38 chr11: 66,630,302-66,630,336 , GRCh37.p13 chr11: 66,397,773-66,397,807 RBM14, RBM14-RBM4
    nsv5545046insertion1nstd206human GRCh38 chr11: 66,615,769-66,615,788 , GRCh37.p13 chr11: 66,383,240-66,383,259 RBM14, RBM14-RBM4
    nsv5497035copy number variation1nstd206human GRCh38 chr11: 66,616,500-66,625,074 , GRCh37.p13 chr11: 66,383,971-66,392,545 RBM14, RBM14-RBM4
    nsv5402653mobile element insertion1nstd206human GRCh38 chr11: 66,626,058-66,626,109 , GRCh37.p13 chr11: 66,393,529-66,393,580 RBM14, RBM14-RBM4
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5139335mobile element insertion1nstd203human GRCh38 chr11: 66,615,720-66,615,769 , GRCh37.p13 chr11: 66,383,191-66,383,240 RBM14, RBM14-RBM4
    nsv5135455mobile element insertion1nstd203human GRCh38 chr11: 66,615,737-66,615,753 , GRCh37.p13 chr11: 66,383,208-66,383,224 RBM14, RBM14-RBM4
    nsv5132340mobile element insertion1nstd203human GRCh38 chr11: 66,615,757-66,615,769 , GRCh37.p13 chr11: 66,383,228-66,383,240 RBM14, RBM14-RBM4
    nsv5128651mobile element insertion1nstd203human GRCh38 chr11: 66,615,753-66,615,769 , GRCh37.p13 chr11: 66,383,224-66,383,240 RBM14-RBM4, RBM14
    nsv5127440mobile element insertion1nstd203human GRCh38 chr11: 66,615,163-66,615,207 , GRCh37.p13 chr11: 66,382,634-66,382,678 RBM14, RBM14-RBM4, 1 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4604927copy number variation1nstd183human GRCh37 chr11: 66,383,979-66,384,738 , GRCh38.p12 chr11: 66,616,508-66,617,267 RBM14-RBM4, RBM14
    nsv4550703insertion1nstd166human GRCh37.p13 chr11: 66,397,756-66,397,756 , GRCh38.p12 chr11: 66,630,285-66,630,285 RBM14, RBM14-RBM4
    nsv4546804insertion1nstd166human GRCh37.p13 chr11: 66,383,224-66,383,224 , GRCh38.p12 chr11: 66,615,753-66,615,753 RBM14-RBM4, RBM14
    nsv4528078copy number variation1nstd166human GRCh37.p13 chr11: 66,396,161-66,396,548 , GRCh38.p12 chr11: 66,628,690-66,629,077 RBM14-RBM4, RBM14
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