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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919479copy number variation1nstd209human GRCh38 chr7: 128,503,915-128,505,178 , GRCh37.p13 chr7: 128,143,969-128,145,232 METTL2B
    nsv5919373copy number variation1nstd209human GRCh38 chr7: 128,505,029-128,505,199 , GRCh37.p13 chr7: 128,145,083-128,145,253 METTL2B
    nsv5914456copy number variation1nstd209human GRCh38 chr7: 128,499,704-128,999,795 , GRCh37.p13 chr7: 128,139,758-128,639,849 , KCP, 25 more genes
    nsv5911762copy number variation1nstd209human GRCh38 chr7: 128,502,791-128,503,260 , GRCh37.p13 chr7: 128,142,845-128,143,314 METTL2B
    nsv5911338copy number variation1nstd209human GRCh38 chr7: 128,499,612-128,999,703 , GRCh37.p13 chr7: 128,139,666-128,639,757 , CICP14, 25 more genes
    nsv5910777copy number variation1nstd209human GRCh38 chr7: 128,499,221-128,499,368 , GRCh37.p13 chr7: 128,139,275-128,139,422 METTL2B
    nsv5694572mobile element insertion1nstd211human GRCh38 chr7: 128,488,289-128,488,289 , GRCh37.p13 chr7: 128,128,343-128,128,343 METTL2B
    nsv5575568copy number variation1nstd207human GRCh38 chr7: 128,489,620-128,489,926 , GRCh37.p13 chr7: 128,129,674-128,129,980 METTL2B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5548491insertion1nstd206human GRCh38 chr7: 128,499,367-128,499,704 , GRCh37.p13 chr7: 128,139,421-128,139,758 METTL2B
    nsv5491753copy number variation1nstd206human GRCh38 chr7: 128,500,077-128,605,280 , GRCh37.p13 chr7: 128,140,131-128,245,334 , METTL2B, 1 more genes
    nsv5485734copy number variation1nstd206human GRCh38 chr7: 128,462,190-128,664,548 , GRCh37.p13 chr7: 128,102,244-128,304,602 , METTL2B, 5 more genes
    nsv5476909copy number variation1nstd206human GRCh38 chr7: 128,496,888-128,499,676 , GRCh37.p13 chr7: 128,136,942-128,139,730 METTL2B
    nsv5475576copy number variation1nstd206human GRCh38 chr7: 128,499,225-128,499,369 , GRCh37.p13 chr7: 128,139,279-128,139,423 METTL2B
    nsv5395483mobile element insertion1nstd206human GRCh38 chr7: 128,488,289-128,488,340 , GRCh37.p13 chr7: 128,128,343-128,128,394 METTL2B
    nsv5336954translocation1nstd200human GRCh37 chr7: 128,142,904-128,142,904 , GRCh37 chr7: 128,143,251-128,143,251 , GRCh38.p12 chr7: 128,503,197-128,503,197 , GRCh38.p12 chr7: 128,502,850-128,502,850 METTL2B
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5117110mobile element insertion1nstd203human GRCh38 chr7: 128,499,650-128,499,687 , GRCh37.p13 chr7: 128,139,704-128,139,741 METTL2B
    nsv5114410mobile element insertion1nstd203human GRCh38 chr7: 128,499,605-128,499,650 , GRCh37.p13 chr7: 128,139,659-128,139,704 METTL2B
    nsv5108367mobile element insertion1nstd203human GRCh38 chr7: 128,499,648-128,499,650 , GRCh37.p13 chr7: 128,139,702-128,139,704 METTL2B
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