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Items: 1 to 20 of 905

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958903insertion1nstd209human GRCh38 chr9: 20,699,767-20,699,767 , GRCh37.p13 chr9: 20,699,766-20,699,766 FOCAD
    nsv5956037insertion1nstd209human GRCh38 chr9: 20,712,138-20,712,138 , GRCh37.p13 chr9: 20,712,137-20,712,137 FOCAD
    nsv5954529insertion1nstd209human GRCh38 chr9: 20,659,440-20,659,440 , GRCh37.p13 chr9: 20,659,439-20,659,439 FOCAD
    nsv5954464insertion1nstd209human GRCh38 chr9: 20,986,266-20,986,266 , GRCh37.p13 chr9: 20,986,265-20,986,265 FOCAD
    nsv5927188copy number variation1nstd209human GRCh38 chr9: 20,809,484-20,809,563 , GRCh37.p13 chr9: 20,809,483-20,809,562 FOCAD
    nsv5922763copy number variation1nstd209human GRCh38 chr9: 20,898,894-20,901,721 , GRCh37.p13 chr9: 20,898,893-20,901,720 FOCAD
    nsv5920741copy number variation1nstd209human GRCh38 chr9: 20,799,592-20,804,617 , GRCh37.p13 chr9: 20,799,591-20,804,616 FOCAD
    nsv5920127copy number variation1nstd209human GRCh38 chr9: 20,856,014-20,860,861 , GRCh37.p13 chr9: 20,856,013-20,860,860 FOCAD
    nsv5915745copy number variation1nstd209human GRCh38 chr9: 20,817,594-20,817,793 , GRCh37.p13 chr9: 20,817,593-20,817,792 FOCAD
    nsv5912528copy number variation1nstd209human GRCh38 chr9: 20,958,300-20,972,584 , GRCh37.p13 chr9: 20,958,299-20,972,583 FOCAD
    nsv5865345copy number variation2nstd209human GRCh38 chr9: 20,958,849-20,960,598 , GRCh37.p13 chr9: 20,958,848-20,960,597 FOCAD
    nsv5865088copy number variation1nstd209human GRCh38 chr9: 20,919,285-20,925,249 , GRCh37.p13 chr9: 20,919,284-20,925,248 FOCAD
    nsv5864955copy number variation1nstd209human GRCh38 chr9: 20,874,315-20,876,514 , GRCh37.p13 chr9: 20,874,314-20,876,513 FOCAD
    nsv5863326copy number variation1nstd209human GRCh38 chr9: 20,915,392-20,921,949 , GRCh37.p13 chr9: 20,915,391-20,921,948 FOCAD
    nsv5862080copy number variation1nstd209human GRCh38 chr9: 20,847,735-20,855,434 , GRCh37.p13 chr9: 20,847,734-20,855,433 FOCAD
    nsv5862036copy number variation1nstd209human GRCh38 chr9: 20,924,700-20,936,968 , GRCh37.p13 chr9: 20,924,699-20,936,967 FOCAD
    nsv5861531copy number variation1nstd209human GRCh38 chr9: 20,958,499-20,969,149 , GRCh37.p13 chr9: 20,958,498-20,969,148 FOCAD
    nsv5860438copy number variation2nstd209human GRCh38 chr9: 20,855,985-20,862,618 , GRCh37.p13 chr9: 20,855,984-20,862,617 FOCAD
    nsv5859910copy number variation1nstd209human GRCh38 chr9: 20,917,992-20,920,877 , GRCh37.p13 chr9: 20,917,991-20,920,876 FOCAD
    nsv5856100copy number variation1nstd209human GRCh38 chr9: 20,843,210-20,886,814 , GRCh37.p13 chr9: 20,843,209-20,886,813 FOCAD
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