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Items: 1 to 20 of 520

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958618insertion1nstd209human GRCh38 chr2: 177,396,942-177,396,942 , GRCh37.p13 chr2: 178,261,670-178,261,670 AGPS
    nsv5953084insertion1nstd209human GRCh38 chr2: 177,486,726-177,486,726 , GRCh37.p13 chr2: 178,351,454-178,351,454 AGPS
    nsv5952661insertion1nstd209human GRCh38 chr2: 177,453,985-177,453,985 , GRCh37.p13 chr2: 178,318,713-178,318,713 AGPS
    nsv5900197copy number variation1nstd209human GRCh38 chr2: 177,422,909-177,423,322 , GRCh37.p13 chr2: 178,287,637-178,288,050 AGPS
    nsv5895563copy number variation1nstd209human GRCh38 chr2: 177,487,060-177,489,447 , GRCh37.p13 chr2: 178,351,788-178,354,175 AGPS
    nsv5888107copy number variation1nstd209human GRCh38 chr2: 177,509,931-177,513,011 , GRCh37.p13 chr2: 178,374,659-178,377,739 AGPS
    nsv5831960copy number variation1nstd209human GRCh38 chr2: 177,509,715-177,513,154 , GRCh37.p13 chr2: 178,374,443-178,377,882 AGPS
    nsv5831959copy number variation1nstd209human GRCh38 chr2: 177,487,156-177,489,563 , GRCh37.p13 chr2: 178,351,884-178,354,291 AGPS
    nsv5690591mobile element insertion2nstd211human GRCh38 chr2: 177,486,738-177,486,738 , GRCh37.p13 chr2: 178,351,466-178,351,466 AGPS
    nsv5688058mobile element insertion1nstd211human GRCh38 chr2: 177,422,621-177,422,621 , GRCh37.p13 chr2: 178,287,349-178,287,349 AGPS
    nsv5676178mobile element insertion2nstd211human GRCh38 chr2: 177,500,493-177,500,493 , GRCh37.p13 chr2: 178,365,221-178,365,221 AGPS
    nsv5617247insertion1nstd207human GRCh38 chr2: 177,450,964-177,450,964 , GRCh37.p13 chr2: 178,315,692-178,315,692 AGPS
    nsv5610044insertion1nstd207human GRCh38 chr2: 177,486,726-177,486,726 , GRCh37.p13 chr2: 178,351,454-178,351,454 AGPS
    nsv5609568insertion1nstd207human GRCh38 chr2: 177,453,985-177,453,985 , GRCh37.p13 chr2: 178,318,713-178,318,713 AGPS
    nsv5566873copy number variation1nstd207human GRCh38 chr2: 177,422,909-177,423,319 , GRCh37.p13 chr2: 178,287,637-178,288,047 AGPS
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5556395sequence alteration1nstd206human GRCh38 chr2: 177,469,137-177,469,147 , GRCh37.p13 chr2: 178,333,865-178,333,875 AGPS
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5535843insertion1nstd206human GRCh38 chr2: 177,469,137-177,469,137 , GRCh37.p13 chr2: 178,333,865-178,333,865 AGPS
    nsv5535672insertion1nstd206human GRCh38 chr2: 177,402,034-177,402,034 , GRCh37.p13 chr2: 178,266,762-178,266,762 AGPS
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