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Items: 1 to 20 of 257

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130314insertion1nstd186human GRCh37 chr19: 7,756,007-7,756,010 , GRCh38.p12 chr19: 7,691,121-7,691,124 FCER2
    nsv5974777insertion1nstd209human GRCh38 chr19: 7,691,122-7,691,122 , GRCh37.p13 chr19: 7,756,008-7,756,008 FCER2
    nsv5938276copy number variation1nstd209human GRCh38 chr19: 7,688,879-7,688,942 , GRCh37.p13 chr19: 7,753,765-7,753,828 FCER2
    nsv5932296copy number variation1nstd209human GRCh38 chr19: 7,692,599-7,692,742 , GRCh37.p13 chr19: 7,757,485-7,757,628 FCER2
    nsv5663220insertion1nstd207human GRCh38 chr19: 7,691,972-7,691,972 , GRCh37.p13 chr19: 7,756,858-7,756,858 FCER2
    nsv5653314insertion1nstd207human GRCh38 chr19: 7,691,051-7,691,051 , GRCh37.p13 chr19: 7,755,937-7,755,937 FCER2
    nsv5597446copy number variation1nstd207human GRCh38 chr19: 7,688,879-7,688,942 , GRCh37.p13 chr19: 7,753,765-7,753,828 FCER2
    nsv5550636insertion1nstd206human GRCh38 chr19: 7,691,121-7,691,124 , GRCh37.p13 chr19: 7,756,007-7,756,010 FCER2
    nsv5523139copy number variation1nstd206human GRCh38 chr19: 7,692,602-7,692,743 , GRCh37.p13 chr19: 7,757,488-7,757,629 FCER2
    nsv5367519translocation1nstd200human GRCh38 chr19: 7,700,822-7,700,822 , GRCh38 chr4: 57,731,655-57,731,655 , GRCh37.p13 chr19: 7,765,708-7,765,708 , GRCh37.p13 chr4: 58,597,821-58,597,821 FCER2
    nsv5328537copy number variation1nstd204human GRCh38.p13 chr19: 7,692,596-7,692,748 , GRCh37.p13 chr19: 7,757,482-7,757,634 FCER2
    nsv5327606copy number variation1nstd204human GRCh37.p13 chr19: 7,731,285-7,786,574 , GRCh38.p13 chr19: 7,666,399-7,721,688 FCER2, RETN, 4 more genes
    nsv5300021copy number variation1nstd204human GRCh38.p13 chr19: 7,690,398-7,692,453 , GRCh37.p13 chr19: 7,755,284-7,757,339 FCER2
    nsv5294104copy number variation1nstd204human GRCh38.p13 chr19: 7,671,601-7,721,400 , GRCh37.p13 chr19: 7,736,487-7,786,286 TRAPPC5, LOC105372262, 2 more genes
    nsv5294004copy number variation1nstd204human GRCh38.p13 chr19: 7,666,644-7,695,815 , GRCh37.p13 chr19: 7,731,530-7,760,701 RPS27AP19, FCER2, 3 more genes
    nsv5292976copy number variation1nstd204human GRCh37.p13 chr19: 7,731,530-7,784,088 , GRCh38.p13 chr19: 7,666,644-7,719,202 FCER2, RETN, 4 more genes
    nsv5292059copy number variation1nstd204human GRCh38.p13 chr19: 7,698,901-7,721,500 , GRCh37.p13 chr19: 7,763,787-7,786,386 FCER2, LOC105372262
    nsv5014450copy number variation1nstd200human GRCh38 chr19: 7,666,561-7,721,490 , GRCh37.p13 chr19: 7,731,447-7,786,376 MCEMP1, LOC105372262, 4 more genes
    nsv4864889copy number variation1nstd200human GRCh37 chr19: 7,755,990-7,757,844 , GRCh38.p12 chr19: 7,691,104-7,692,958 FCER2
    nsv4864888copy number variation1nstd200human GRCh37 chr19: 7,731,443-7,786,376 , GRCh38.p12 chr19: 7,666,557-7,721,490 TRAPPC5, RPS27AP19, 4 more genes
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