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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116946mobile element insertion1nstd186human GRCh37 chr6: 31,026,614-31,026,665 , GRCh38.p12 chr6: 31,058,837-31,058,888 HCG22
    nsv5894857copy number variation1nstd209human GRCh38 chr6: 31,055,484-31,055,879 , GRCh37.p13 chr6: 31,023,261-31,023,656 HCG22
    nsv5725193mobile element insertion1nstd211human GRCh38 chr6: 31,058,837-31,058,837 , GRCh37.p13 chr6: 31,026,614-31,026,614 HCG22
    nsv5678571mobile element insertion2nstd211human GRCh38 chr6: 31,058,837-31,058,837 , GRCh37.p13 chr6: 31,026,614-31,026,614 HCG22
    nsv5641524insertion1nstd207human GRCh38 chr6: 31,058,824-31,058,824 , GRCh37.p13 chr6: 31,026,601-31,026,601 HCG22
    nsv5571686copy number variation1nstd207human GRCh38 chr6: 31,055,484-31,055,879 , GRCh37.p13 chr6: 31,023,261-31,023,656 HCG22
    nsv5404458mobile element insertion1nstd206human GRCh38 chr6: 31,058,837-31,058,888 , GRCh37.p13 chr6: 31,026,614-31,026,665 HCG22
    nsv5387076copy number variation1nstd186human GRCh37 chr6: 31,023,261-31,023,657 , GRCh38.p12 chr6: 31,055,484-31,055,880 HCG22
    nsv5307713copy number variation1nstd204human GRCh38.p13 chr6: 31,055,483-31,055,881 , GRCh37.p13 chr6: 31,023,260-31,023,658 HCG22
    nsv5302105copy number variation1nstd204human GRCh38.p13 chr6: 31,055,453-31,055,682 , GRCh37.p13 chr6: 31,023,230-31,023,459 HCG22
    nsv5239129copy number variation1nstd204human GRCh38.p13 chr6: 31,055,501-31,055,900 , GRCh37.p13 chr6: 31,023,278-31,023,677 HCG22
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5116437mobile element insertion1nstd203human GRCh38 chr6: 31,058,828-31,058,833 , GRCh37.p13 chr6: 31,026,605-31,026,610 HCG22
    nsv5107521mobile element insertion1nstd203human GRCh38 chr6: 31,058,831-31,058,837 , GRCh37.p13 chr6: 31,026,608-31,026,614 HCG22
    nsv5103524mobile element insertion1nstd203human GRCh38 chr6: 31,058,165-31,058,180 , GRCh37.p13 chr6: 31,025,942-31,025,957 HCG22
    nsv5103263mobile element insertion1nstd203human GRCh38 chr6: 31,058,824-31,058,834 , GRCh37.p13 chr6: 31,026,601-31,026,611 HCG22
    nsv4940661copy number variation1nstd200human GRCh38 chr6: 31,047,739-31,064,812 , GRCh37.p13 chr6: 31,015,516-31,032,589 HCG22
    nsv4940660copy number variation1nstd200human GRCh38 chr6: 31,042,762-31,065,423 , GRCh37.p13 chr6: 31,010,539-31,033,200 HCG22
    nsv4934576copy number variation1nstd200human GRCh38 chr6: 31,051,983-31,059,235 , GRCh37.p13 chr6: 31,019,760-31,027,012 HCG22
    nsv4828595copy number variation1nstd200human GRCh37 chr6: 31,019,760-31,027,012 , GRCh38.p12 chr6: 31,051,983-31,059,235 HCG22
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