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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945687copy number variation1nstd209human GRCh38 chr13: 64,069,219-64,079,653 , GRCh37.p13 chr13: 64,643,352-64,653,786 LINC00355
    nsv5944317copy number variation1nstd209human GRCh38 chr13: 64,029,990-64,030,435 , GRCh37.p13 chr13: 64,604,123-64,604,568 LINC00355
    nsv5865833copy number variation1nstd209human GRCh38 chr13: 64,069,180-64,076,768 , GRCh37.p13 chr13: 64,643,313-64,650,901 LINC00355
    nsv5850129copy number variation1nstd209human GRCh38 chr13: 64,074,588-64,079,018 , GRCh37.p13 chr13: 64,648,721-64,653,151 LINC00355
    nsv5728383mobile element insertion1nstd211human GRCh38 chr13: 64,024,865-64,024,865 , GRCh37.p13 chr13: 64,598,998-64,598,998 LINC00355
    nsv5726013mobile element insertion1nstd211human GRCh38 chr13: 64,003,865-64,003,865 , GRCh37.p13 chr13: 64,577,998-64,577,998 LINC00355
    nsv5722004mobile element insertion2nstd211human GRCh38 chr13: 63,995,722-63,995,722 , GRCh37.p13 chr13: 64,569,855-64,569,855 LINC00355
    nsv5719242mobile element insertion1nstd211human GRCh38 chr13: 64,017,600-64,017,600 , GRCh37.p13 chr13: 64,591,733-64,591,733 LINC00355
    nsv5713473mobile element insertion2nstd211human GRCh38 chr13: 64,046,362-64,046,362 , GRCh37.p13 chr13: 64,620,495-64,620,495 LINC00355
    nsv5711804mobile element insertion2nstd211human GRCh38 chr13: 63,985,140-63,985,140 , GRCh37.p13 chr13: 64,559,273-64,559,273 LINC00355
    nsv5707274mobile element insertion2nstd211human GRCh38 chr13: 64,066,082-64,066,082 , GRCh37.p13 chr13: 64,640,215-64,640,215 LINC00355
    nsv5707093mobile element insertion1nstd211human GRCh38 chr13: 64,010,222-64,010,222 , GRCh37.p13 chr13: 64,584,355-64,584,355 LINC00355
    nsv5648960insertion1nstd207human GRCh38 chr13: 63,995,704-63,995,704 , GRCh37.p13 chr13: 64,569,837-64,569,837 LINC00355
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5502560copy number variation1nstd206human GRCh38 chr13: 63,817,163-65,941,403 , GRCh37.p13 chr13: 64,391,296-66,515,535 LGMNP1, OR7E104P, 15 more genes
    nsv5499725copy number variation1nstd206human GRCh38 chr13: 64,070,689-64,070,839 , GRCh37.p13 chr13: 64,644,822-64,644,972 LINC00355
    nsv5432471mobile element insertion1nstd206human GRCh38 chr13: 64,010,222-64,010,273 , GRCh37.p13 chr13: 64,584,355-64,584,406 LINC00355
    nsv5429923mobile element insertion1nstd206human GRCh38 chr13: 64,066,082-64,066,133 , GRCh37.p13 chr13: 64,640,215-64,640,266 LINC00355
    nsv5429631mobile element insertion1nstd206human GRCh38 chr13: 63,985,140-63,985,191 , GRCh37.p13 chr13: 64,559,273-64,559,324 LINC00355
    nsv5422580mobile element insertion1nstd206human GRCh38 chr13: 64,046,362-64,046,413 , GRCh37.p13 chr13: 64,620,495-64,620,546 LINC00355
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