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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941649copy number variation1nstd209human GRCh38 chr14: 32,086,493-32,086,930 , GRCh37.p13 chr14: 32,555,699-32,556,136 ARHGAP5
    nsv5934464copy number variation1nstd209human GRCh38 chr14: 32,138,155-32,138,275 , GRCh37.p13 chr14: 32,607,361-32,607,481 ARHGAP5
    nsv5853362copy number variation1nstd209human GRCh38 chr14: 32,112,377-32,115,455 , GRCh37.p13 chr14: 32,581,583-32,584,661 ARHGAP5
    nsv5730173mobile element insertion1nstd211human GRCh38 chr14: 32,087,486-32,087,486 , GRCh37.p13 chr14: 32,556,692-32,556,692 ARHGAP5
    nsv5724337mobile element insertion1nstd211human GRCh38 chr14: 32,081,269-32,081,269 , GRCh37.p13 chr14: 32,550,475-32,550,475 ARHGAP5
    nsv5714631mobile element insertion1nstd211human GRCh38 chr14: 32,130,890-32,130,890 , GRCh37.p13 chr14: 32,600,096-32,600,096 ARHGAP5
    nsv5600770copy number variation1nstd207human GRCh38 chr14: 32,086,493-32,086,930 , GRCh37.p13 chr14: 32,555,699-32,556,136 ARHGAP5
    nsv5555698mobile element insertion1nstd206human GRCh38 chr14: 32,081,269-32,081,281 , GRCh37.p13 chr14: 32,550,475-32,550,487 ARHGAP5
    nsv5539083insertion1nstd206human GRCh38 chr14: 32,154,469-32,154,475 , GRCh37.p13 chr14: 32,623,675-32,623,681 ARHGAP5
    nsv5513095copy number variation1nstd206human GRCh38 chr14: 32,136,827-32,136,895 , GRCh37.p13 chr14: 32,606,033-32,606,101 ARHGAP5
    nsv5512475copy number variation1nstd206human GRCh38 chr14: 32,122,529-32,123,502 , GRCh37.p13 chr14: 32,591,735-32,592,708 ARHGAP5
    nsv5506089copy number variation1nstd206human GRCh38 chr14: 32,138,158-32,138,276 , GRCh37.p13 chr14: 32,607,364-32,607,482 ARHGAP5
    nsv5498763copy number variation1nstd206human GRCh38 chr14: 32,086,496-32,086,931 , GRCh37.p13 chr14: 32,555,702-32,556,137 ARHGAP5
    nsv5357063translocation1nstd200human GRCh38 chr14: 32,138,158-32,138,158 , GRCh38 chr14: 32,138,276-32,138,276 , GRCh37.p13 chr14: 32,607,482-32,607,482 , GRCh37.p13 chr14: 32,607,364-32,607,364 ARHGAP5
    nsv5357062translocation1nstd200human GRCh38 chr14: 32,086,496-32,086,496 , GRCh38 chr14: 32,086,931-32,086,931 , GRCh37.p13 chr14: 32,555,702-32,555,702 , GRCh37.p13 chr14: 32,556,137-32,556,137 ARHGAP5
    nsv5345373translocation1nstd200human GRCh37 chr14: 32,556,137-32,556,137 , GRCh37 chr14: 32,555,702-32,555,702 , GRCh38.p12 chr14: 32,086,496-32,086,496 , GRCh38.p12 chr14: 32,086,931-32,086,931 ARHGAP5
    nsv5302279copy number variation1nstd204human GRCh38.p13 chr14: 32,094,908-32,095,316 , GRCh37.p13 chr14: 32,564,114-32,564,522 ARHGAP5
    nsv5273007copy number variation1nstd204human GRCh38.p13 chr14: 32,155,401-32,160,600 , GRCh37.p13 chr14: 32,624,607-32,629,806 ARHGAP5
    nsv4994175copy number variation1nstd200human GRCh38 chr14: 32,083,469-32,086,983 , GRCh37.p13 chr14: 32,552,675-32,556,189 ARHGAP5
    nsv4845932copy number variation1nstd200human GRCh37 chr14: 32,581,886-32,584,619 , GRCh38.p12 chr14: 32,112,680-32,115,413 ARHGAP5
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