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Items: 1 to 20 of 349

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118011copy number variation1nstd186human GRCh37 chr6: 119,165,051-119,169,931 , GRCh38.p12 chr6: 118,843,888-118,848,768 MCM9
    nsv5966535insertion1nstd209human GRCh38 chr6: 118,843,654-118,843,654 , GRCh37.p13 chr6: 119,164,817-119,164,817 MCM9
    nsv5964152insertion1nstd209human GRCh38 chr6: 118,869,599-118,869,599 , GRCh37.p13 chr6: 119,190,764-119,190,764 MCM9
    nsv5952121insertion1nstd209human GRCh38 chr6: 118,933,964-118,933,964 , GRCh37.p13 chr6: 119,255,129-119,255,129 MCM9
    nsv5904271copy number variation1nstd209human GRCh38 chr6: 118,852,730-118,853,441 , GRCh37.p13 chr6: 119,173,893-119,174,604 MCM9
    nsv5903427copy number variation1nstd209human GRCh38 chr6: 118,848,914-118,851,805 , GRCh37.p13 chr6: 119,170,077-119,172,968 MCM9
    nsv5894560copy number variation1nstd209human GRCh38 chr6: 118,843,886-118,848,720 , GRCh37.p13 chr6: 119,165,049-119,169,883 MCM9
    nsv5844238copy number variation1nstd209human GRCh38 chr6: 118,843,912-118,851,688 , GRCh37.p13 chr6: 119,165,075-119,172,851 MCM9
    nsv5723544mobile element insertion1nstd211human GRCh38 chr6: 118,881,955-118,881,955 , GRCh37.p13 chr6: 119,203,120-119,203,120 MCM9
    nsv5689133mobile element insertion1nstd211human GRCh38 chr6: 118,837,092-118,837,092 , GRCh37.p13 chr6: 119,158,255-119,158,255 MCM9
    nsv5675685mobile element insertion1nstd211human GRCh38 chr6: 118,933,983-118,933,983 , GRCh37.p13 chr6: 119,255,148-119,255,148 MCM9
    nsv5638936insertion1nstd207human GRCh38 chr6: 118,843,641-118,843,641 , GRCh37.p13 chr6: 119,164,804-119,164,804 MCM9
    nsv5473701copy number variation1nstd206human GRCh38 chr6: 118,848,768-118,851,806 , GRCh37.p13 chr6: 119,169,931-119,172,969 MCM9
    nsv5470031copy number variation1nstd206human GRCh38 chr6: 118,537,253-118,822,880 , GRCh37.p13 chr6: 118,858,416-119,144,043 PLN, MCM9, 4 more genes
    nsv5462354copy number variation1nstd206human GRCh38 chr6: 118,843,888-118,848,768 , GRCh37.p13 chr6: 119,165,051-119,169,931 MCM9
    nsv5460739copy number variation1nstd206human GRCh38 chr6: 118,852,730-118,853,442 , GRCh37.p13 chr6: 119,173,893-119,174,605 MCM9
    nsv5457610copy number variation1nstd206human GRCh38 chr6: 118,818,109-118,834,872 , GRCh37.p13 chr6: 119,139,272-119,156,035 MCM9
    nsv5404252mobile element insertion1nstd206human GRCh38 chr6: 118,837,092-118,837,143 , GRCh37.p13 chr6: 119,158,255-119,158,306 MCM9
    nsv5389071copy number variation1nstd186human GRCh37 chr6: 119,165,054-119,172,967 , GRCh38.p12 chr6: 118,843,891-118,851,804 MCM9
    nsv5385883copy number variation1nstd186human GRCh37 chr6: 119,165,052-119,172,967 , GRCh38.p12 chr6: 118,843,889-118,851,804 MCM9
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