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Items: 1 to 20 of 362

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961275insertion1nstd209human GRCh38 chr7: 139,106,851-139,106,851 , GRCh37.p13 chr7: 138,791,597-138,791,597 ZC3HAV1
    nsv5948440insertion1nstd209human GRCh38 chr7: 139,097,415-139,097,415 , GRCh37.p13 chr7: 138,782,161-138,782,161 ZC3HAV1
    nsv5925984copy number variation1nstd209human GRCh38 chr7: 139,092,583-139,093,859 , GRCh37.p13 chr7: 138,777,329-138,778,605 ZC3HAV1
    nsv5922998copy number variation1nstd209human GRCh38 chr7: 139,057,522-139,057,838 , GRCh37.p13 chr7: 138,742,268-138,742,584 ZC3HAV1
    nsv5922938copy number variation1nstd209human GRCh38 chr7: 139,070,596-139,070,691 , GRCh37.p13 chr7: 138,755,342-138,755,437 ZC3HAV1
    nsv5706991mobile element insertion2nstd211human GRCh38 chr7: 139,106,866-139,106,866 , GRCh37.p13 chr7: 138,791,612-138,791,612 ZC3HAV1
    nsv5638408insertion1nstd207human GRCh38 chr7: 139,106,851-139,106,851 , GRCh37.p13 chr7: 138,791,597-138,791,597 ZC3HAV1
    nsv5628544insertion1nstd207human GRCh38 chr7: 139,101,478-139,101,478 , GRCh37.p13 chr7: 138,786,224-138,786,224 ZC3HAV1
    nsv5577936copy number variation1nstd207human GRCh38 chr7: 139,057,522-139,057,838 , GRCh37.p13 chr7: 138,742,268-138,742,584 ZC3HAV1
    nsv5570185copy number variation1nstd207human GRCh38 chr7: 139,100,755-139,100,804 , GRCh37.p13 chr7: 138,785,501-138,785,550 ZC3HAV1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5491348copy number variation1nstd206human GRCh38 chr7: 139,070,601-139,070,692 , GRCh37.p13 chr7: 138,755,347-138,755,438 ZC3HAV1
    nsv5490700copy number variation1nstd206human GRCh38 chr7: 139,108,148-139,108,232 , GRCh37.p13 chr7: 138,792,894-138,792,978 ZC3HAV1
    nsv5485473copy number variation1nstd206human GRCh38 chr7: 139,057,536-139,057,839 , GRCh37.p13 chr7: 138,742,282-138,742,585 ZC3HAV1
    nsv5412724mobile element insertion1nstd206human GRCh38 chr7: 139,106,866-139,106,917 , GRCh37.p13 chr7: 138,791,612-138,791,663 ZC3HAV1
    nsv5382384mobile element deletion2nstd186human GRCh37 chr7: 138,742,282-138,742,585 , GRCh38.p12 chr7: 139,057,536-139,057,839 ZC3HAV1
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5255431copy number variation1nstd204human GRCh38.p13 chr7: 139,057,501-139,057,800 , GRCh37.p13 chr7: 138,742,247-138,742,546 ZC3HAV1
    nsv5217754mobile element deletion1nstd204human GRCh38.p13 chr7: 139,057,536-139,057,839 , GRCh37.p13 chr7: 138,742,282-138,742,585 ZC3HAV1
    nsv5119732mobile element insertion1nstd203human GRCh38 chr7: 139,106,866-139,106,866 , GRCh37.p13 chr7: 138,791,612-138,791,612 ZC3HAV1
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