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Items: 1 to 20 of 596

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972650inversion1nstd209human GRCh38 chr1: 229,174,728-232,234,598 , GRCh37.p13 chr1: 229,310,475-232,370,344 , ACTA1, 68 more genes
    nsv5971633inversion1nstd209human GRCh38 chr1: 229,416,331-231,831,980 , GRCh37.p13 chr1: 229,552,078-231,967,726 , ACTA1, 56 more genes
    nsv5962535insertion1nstd209human GRCh38 chr1: 230,127,537-230,127,537 , GRCh37.p13 chr1: 230,263,284-230,263,284 GALNT2
    nsv5950597insertion1nstd209human GRCh38 chr1: 230,222,031-230,222,031 , GRCh37.p13 chr1: 230,357,777-230,357,777 GALNT2
    nsv5885404copy number variation1nstd209human GRCh38 chr1: 230,077,601-230,081,615 , GRCh37.p13 chr1: 230,213,348-230,217,362 GALNT2
    nsv5883900copy number variation1nstd209human GRCh38 chr1: 230,103,140-230,108,098 , GRCh37.p13 chr1: 230,238,887-230,243,845 GALNT2
    nsv5876121copy number variation1nstd209human GRCh38 chr1: 230,272,967-230,273,747 , GRCh37.p13 chr1: 230,408,713-230,409,493 GALNT2
    nsv5874161copy number variation1nstd209human GRCh38 chr1: 230,082,983-230,083,069 , GRCh37.p13 chr1: 230,218,730-230,218,816 GALNT2
    nsv5870443copy number variation1nstd209human GRCh38 chr1: 230,227,439-230,227,510 , GRCh37.p13 chr1: 230,363,185-230,363,256 GALNT2
    nsv5868340copy number variation1nstd209human GRCh38 chr1: 230,187,852-230,187,944 , GRCh37.p13 chr1: 230,323,598-230,323,690 GALNT2
    nsv5829474copy number variation1nstd209human GRCh38 chr1: 230,077,454-230,081,653 , GRCh37.p13 chr1: 230,213,201-230,217,400 GALNT2
    nsv5829239copy number variation1nstd209human GRCh38 chr1: 230,102,978-230,108,111 , GRCh37.p13 chr1: 230,238,725-230,243,858 GALNT2
    nsv5717191mobile element insertion2nstd211human GRCh38 chr1: 230,105,847-230,105,847 , GRCh37.p13 chr1: 230,241,594-230,241,594 GALNT2
    nsv5692215mobile element insertion1nstd211human GRCh38 chr1: 230,149,610-230,149,610 , GRCh37.p13 chr1: 230,285,357-230,285,357 GALNT2
    nsv5689290mobile element insertion2nstd211human GRCh38 chr1: 230,119,302-230,119,302 , GRCh37.p13 chr1: 230,255,049-230,255,049 GALNT2
    nsv5618901insertion1nstd207human GRCh38 chr1: 230,198,476-230,198,476 , GRCh37.p13 chr1: 230,334,222-230,334,222 GALNT2
    nsv5618886insertion1nstd207human GRCh38 chr1: 230,127,537-230,127,537 , GRCh37.p13 chr1: 230,263,284-230,263,284 GALNT2
    nsv5616133insertion1nstd207human GRCh38 chr1: 230,119,289-230,119,289 , GRCh37.p13 chr1: 230,255,036-230,255,036 GALNT2
    nsv5572364copy number variation1nstd207human GRCh38 chr1: 230,275,958-230,276,036 , GRCh37.p13 chr1: 230,411,704-230,411,782 GALNT2
    nsv5570385copy number variation1nstd207human GRCh38 chr1: 230,198,359-230,198,475 , GRCh37.p13 chr1: 230,334,105-230,334,221 GALNT2
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