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Items: 1 to 20 of 399

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969343inversion1nstd209human GRCh38 chr1: 161,566,673-161,918,703 , GRCh37.p13 chr1: 161,536,463-161,888,493 FCGR2B, FCGR3B, 12 more genes
    nsv5955969insertion1nstd209human GRCh38 chr1: 161,920,294-161,920,294 , GRCh37.p13 chr1: 161,890,084-161,890,084 ATF6
    nsv5953536insertion1nstd209human GRCh38 chr1: 161,868,759-161,868,759 , GRCh37.p13 chr1: 161,838,549-161,838,549 ATF6
    nsv5881058copy number variation1nstd209human GRCh38 chr1: 161,697,901-161,830,547 , GRCh37.p13 chr1: 161,667,691-161,800,337 DUSP12, ATF6, 4 more genes
    nsv5828705copy number variation1nstd209human GRCh38 chr1: 161,916,691-161,984,740 , GRCh37.p13 chr1: 161,886,481-161,954,530 ATF6, OLFML2B
    nsv5828704copy number variation1nstd209human GRCh38 chr1: 161,831,321-161,834,274 , GRCh37.p13 chr1: 161,801,111-161,804,064 ATF6
    nsv5828503copy number variation1nstd209human GRCh38 chr1: 161,821,496-161,929,487 , GRCh37.p13 chr1: 161,791,286-161,899,277 ATF6, LOC100422526
    nsv5828502copy number variation1nstd209human GRCh38 chr1: 161,819,484-161,825,524 , GRCh37.p13 chr1: 161,789,274-161,795,314 ATF6
    nsv5828501copy number variation1nstd209human GRCh38 chr1: 161,803,607-161,805,825 , GRCh37.p13 chr1: 161,773,397-161,775,615 ATF6
    nsv5729015mobile element insertion1nstd211human GRCh38 chr1: 161,873,264-161,873,264 , GRCh37.p13 chr1: 161,843,054-161,843,054 ATF6
    nsv5717514mobile element insertion2nstd211human GRCh38 chr1: 161,780,224-161,780,224 , GRCh37.p13 chr1: 161,750,014-161,750,014 ATF6
    nsv5694273mobile element insertion1nstd211human GRCh38 chr1: 161,894,099-161,894,099 , GRCh37.p13 chr1: 161,863,889-161,863,889 ATF6
    nsv5682239mobile element insertion1nstd211human GRCh38 chr1: 161,842,056-161,842,056 , GRCh37.p13 chr1: 161,811,846-161,811,846 ATF6
    nsv5681357mobile element insertion2nstd211human GRCh38 chr1: 161,868,768-161,868,768 , GRCh37.p13 chr1: 161,838,558-161,838,558 ATF6
    nsv5674991mobile element insertion2nstd211human GRCh38 chr1: 161,803,154-161,803,154 , GRCh37.p13 chr1: 161,772,944-161,772,944 ATF6
    nsv5432265copy number variation1nstd206human GRCh38 chr1: 161,831,431-161,834,346 , GRCh37.p13 chr1: 161,801,221-161,804,136 ATF6
    nsv5427206copy number variation1nstd206human GRCh38 chr1: 161,923,728-161,923,787 , GRCh37.p13 chr1: 161,893,518-161,893,577 ATF6
    nsv5426806copy number variation1nstd206human GRCh38 chr1: 161,833,766-161,834,981 , GRCh37.p13 chr1: 161,803,556-161,804,771 ATF6
    nsv5422552copy number variation1nstd206human GRCh38 chr1: 161,917,569-161,920,443 , GRCh37.p13 chr1: 161,887,359-161,890,233 ATF6
    nsv5413326mobile element insertion1nstd206human GRCh38 chr1: 161,868,768-161,868,819 , GRCh37.p13 chr1: 161,838,558-161,838,609 ATF6
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