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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116937mobile element insertion1nstd186human GRCh37 chr20: 1,147,982-1,148,033 , GRCh38.p12 chr20: 1,167,338-1,167,389 PSMF1
    nsv5980203insertion1nstd209human GRCh38 chr20: 1,133,569-1,133,569 , GRCh37.p13 chr20: 1,114,212-1,114,212 PSMF1
    nsv5977745insertion1nstd209human GRCh38 chr20: 1,167,321-1,167,321 , GRCh37.p13 chr20: 1,147,965-1,147,965 PSMF1
    nsv5941690copy number variation1nstd209human GRCh38 chr20: 1,114,552-1,115,275 , GRCh37.p13 chr20: 1,095,195-1,095,918 PSMF1
    nsv5704584mobile element insertion1nstd211human GRCh38 chr20: 1,145,480-1,145,480 , GRCh37.p13 chr20: 1,126,123-1,126,123 PSMF1
    nsv5701765mobile element insertion2nstd211human GRCh38 chr20: 1,167,338-1,167,338 , GRCh37.p13 chr20: 1,147,982-1,147,982 PSMF1
    nsv5663954insertion1nstd207human GRCh38 chr20: 1,149,893-1,149,893 , GRCh37.p13 chr20: 1,130,536-1,130,536 PSMF1
    nsv5663359insertion1nstd207human GRCh38 chr20: 1,149,837-1,149,837 , GRCh37.p13 chr20: 1,130,480-1,130,480 PSMF1
    nsv5661861insertion1nstd207human GRCh38 chr20: 1,150,048-1,150,048 , GRCh37.p13 chr20: 1,130,691-1,130,691 PSMF1
    nsv5655024insertion1nstd207human GRCh38 chr20: 1,114,732-1,114,732 , GRCh37.p13 chr20: 1,095,375-1,095,375 PSMF1
    nsv5603297copy number variation1nstd207human GRCh38 chr20: 1,114,753-1,114,829 , GRCh37.p13 chr20: 1,095,396-1,095,472 PSMF1
    nsv5603289copy number variation1nstd207human GRCh38 chr20: 1,114,495-1,114,571 , GRCh37.p13 chr20: 1,095,138-1,095,214 PSMF1
    nsv5602637copy number variation1nstd207human GRCh38 chr20: 1,114,495-1,114,951 , GRCh37.p13 chr20: 1,095,138-1,095,594 PSMF1
    nsv5600617copy number variation1nstd207human GRCh38 chr20: 1,149,984-1,150,138 , GRCh37.p13 chr20: 1,130,627-1,130,781 PSMF1
    nsv5536282insertion1nstd206human GRCh38 chr20: 1,133,537-1,133,575 , GRCh37.p13 chr20: 1,114,180-1,114,218 PSMF1
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5529362copy number variation1nstd206human GRCh38 chr20: 1,149,353-1,150,685 , GRCh37.p13 chr20: 1,129,996-1,131,328 PSMF1
    nsv5518821copy number variation1nstd206human GRCh38 chr20: 1,168,994-1,169,103 , GRCh37.p13 chr20: 1,149,638-1,149,747 PSMF1
    nsv5515758copy number variation1nstd206human GRCh38 chr20: 1,161,022-1,161,130 , GRCh37.p13 chr20: 1,141,666-1,141,774 ACTG1P3, PSMF1
    nsv5416566mobile element insertion1nstd206human GRCh38 chr20: 1,145,480-1,145,531 , GRCh37.p13 chr20: 1,126,123-1,126,174 PSMF1
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