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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869717copy number variation1nstd209human GRCh38 chr19: 42,100,022-42,102,076 , GRCh37.p13 chr19: 42,604,174-42,606,228 POU2F2
    nsv5697598mobile element insertion1nstd211human GRCh38 chr19: 42,085,301-42,085,301 , GRCh37.p13 chr19: 42,589,453-42,589,453 POU2F2
    nsv5564519copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,987,984-42,252,574 , GRCh37.p13 chr19: 42,514,712-42,756,726 GRIK5, DEDD2, 8 more genes
    nsv5564317copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,983,952-42,247,520 , GRCh37.p13 chr19: 42,514,712-42,751,672 GSK3A, ZNF574, 8 more genes
    nsv5564233copy number variation1nstd102humanPathogenic GRCh38 chr19: 42,032,860-42,297,536 , GRCh37.p13 chr19: 42,537,012-42,801,688 POU2F2, ERF, 9 more genes
    nsv5564232copy number variation1nstd102humanPathogenic GRCh38 chr19: 41,952,441-42,266,625 , GRCh37.p13 chr19: 42,514,712-42,770,777 CIC, ERF, 10 more genes
    nsv5562413sequence alteration1nstd206human GRCh38 chr19: 41,797,706-42,527,281 , GRCh37.p13 chr19: 42,514,712-43,031,433 MEGF8, LIPE, 34 more genes
    nsv5554149sequence alteration1nstd206human GRCh38 chr19: 41,749,279-42,444,786 , GRCh37.p13 chr19: 42,514,712-42,948,938 ERF, CEACAM6, 32 more genes
    nsv5532732copy number variation1nstd206human GRCh38 chr19: 42,176,350-42,176,401 , GRCh37.p13 chr19: 42,680,502-42,680,553 POU2F2
    nsv5342002translocation1nstd200human GRCh37 chr19: 42,699,010-42,699,010 , GRCh37 chr19: 42,699,295-42,699,295 , GRCh38.p12 chr19: 42,195,143-42,195,143 , GRCh38.p12 chr19: 42,194,858-42,194,858 POU2F2
    nsv5337630translocation1nstd200human GRCh37 chr19: 42,699,143-42,699,143 , GRCh37 chr19: 42,699,007-42,699,007 , GRCh38.p12 chr19: 42,194,991-42,194,991 , GRCh38.p12 chr19: 42,194,855-42,194,855 POU2F2
    nsv5291689copy number variation1nstd204human GRCh38.p13 chr19: 42,095,433-42,096,696 , GRCh37.p13 chr19: 42,599,585-42,600,848 POU2F2
    nsv5214483mobile element deletion1nstd204human GRCh38.p13 chr19: 42,103,603-42,103,959 , GRCh37.p13 chr19: 42,607,755-42,608,111 POU2F2
    nsv5172159mobile element insertion1nstd203human GRCh38 chr19: 42,192,594-42,192,608 , GRCh37.p13 chr19: 42,696,746-42,696,760 POU2F2
    nsv5020517copy number variation1nstd200human GRCh38 chr19: 42,160,097-42,160,842 , GRCh37.p13 chr19: 42,664,249-42,664,994 POU2F2
    nsv5020516copy number variation1nstd200human GRCh38 chr19: 42,100,036-42,100,124 , GRCh37.p13 chr19: 42,604,188-42,604,276 POU2F2
    nsv4868448copy number variation1nstd200human GRCh37 chr19: 42,604,188-42,604,276 , GRCh38.p12 chr19: 42,100,036-42,100,124 POU2F2
    nsv4769822mobile element deletion1nstd200human GRCh37 chr19: 42,607,782-42,608,084 , GRCh38.p12 chr19: 42,103,630-42,103,932 POU2F2
    nsv4716349inversion1nstd195human GRCh37 chr19: 42,597,139-42,597,140 , GRCh38.p12 chr19: 42,092,987-42,092,988 POU2F2
    nsv4701913copy number variation1nstd195human GRCh38.p12 chr19: 42,014,849-42,223,099 , GRCh37 chr19: 42,519,001-42,727,251 GRIK5, POU2F2, 5 more genes
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