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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5862016copy number variation1nstd209human GRCh38 chr11: 11,194,943-11,198,979 , GRCh37.p13 chr11: 11,216,490-11,220,526 LINC02752
    nsv5724063mobile element insertion2nstd211human GRCh38 chr11: 11,129,826-11,129,826 , GRCh37.p13 chr11: 11,151,373-11,151,373 LINC02752
    nsv5712464mobile element insertion1nstd211human GRCh38 chr11: 11,202,099-11,202,099 , GRCh37.p13 chr11: 11,223,646-11,223,646 LINC02752
    nsv5701890mobile element insertion1nstd211human GRCh38 chr11: 11,207,721-11,207,721 , GRCh37.p13 chr11: 11,229,268-11,229,268 LINC02752
    nsv5698043mobile element insertion1nstd211human GRCh38 chr11: 11,202,086-11,202,086 , GRCh37.p13 chr11: 11,223,633-11,223,633 LINC02752
    nsv5660694insertion1nstd207human GRCh38 chr11: 11,177,044-11,177,044 , GRCh37.p13 chr11: 11,198,591-11,198,591 LINC02752
    nsv5653692insertion1nstd207human GRCh38 chr11: 11,129,811-11,129,811 , GRCh37.p13 chr11: 11,151,358-11,151,358 LINC02752
    nsv5561061mobile element insertion1nstd206human GRCh38 chr11: 11,129,826-11,129,877 , GRCh37.p13 chr11: 11,151,373-11,151,424 LINC02752
    nsv5509579copy number variation1nstd206human GRCh38 chr11: 11,133,648-11,138,971 , GRCh37.p13 chr11: 11,155,195-11,160,518 , LOC100288365, 1 more genes
    nsv5496247copy number variation1nstd206human GRCh38 chr11: 11,204,346-11,204,442 , GRCh37.p13 chr11: 11,225,893-11,225,989 LINC02752
    nsv5411400mobile element insertion1nstd206human GRCh38 chr11: 11,202,036-11,202,086 , GRCh37.p13 chr11: 11,223,583-11,223,633 LINC02752
    nsv5393820mobile element deletion1nstd186human GRCh37 chr11: 11,216,078-11,220,403 , GRCh38.p12 chr11: 11,194,531-11,198,856 LINC02752
    nsv5393623mobile element deletion1nstd186human GRCh37 chr11: 11,216,073-11,220,400 , GRCh38.p12 chr11: 11,194,526-11,198,853 LINC02752
    nsv5354731translocation1nstd200human GRCh38 chr11: 11,171,340-11,171,340 , GRCh38 chr11: 11,171,412-11,171,412 , GRCh37.p13 chr11: 11,192,887-11,192,887 , GRCh37.p13 chr11: 11,192,959-11,192,959 LINC02752
    nsv5324016mobile element deletion1nstd204human GRCh38.p13 chr11: 11,194,501-11,198,886 , GRCh37.p13 chr11: 11,216,048-11,220,433 LINC02752
    nsv5321366inversion1nstd204human GRCh38.p13 chr11: 11,161,297-11,161,766 , GRCh37.p13 chr11: 11,182,844-11,183,313 LINC02752
    nsv5320823inversion1nstd204human GRCh38.p13 chr11: 11,161,406-11,161,767 , GRCh37.p13 chr11: 11,182,953-11,183,314 LINC02752
    nsv5257273copy number variation1nstd204human GRCh38.p13 chr11: 11,135,059-11,137,437 , GRCh37.p13 chr11: 11,156,606-11,158,984 , LOC100288365, 1 more genes
    nsv5256083copy number variation1nstd204human GRCh38.p13 chr11: 11,194,005-11,199,196 , GRCh37.p13 chr11: 11,215,552-11,220,743 LINC02752
    nsv5251446copy number variation1nstd204human GRCh38.p13 chr11: 11,192,801-11,199,200 , GRCh37.p13 chr11: 11,214,348-11,220,747 LINC02752
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