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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv5972210inversion1nstd209human GRCh38 chr9: 36,238,245-37,822,315 , GRCh37.p13 chr9: 36,238,242-37,822,312 PAX5, GRHPR, 35 more genes
    nsv5969677inversion1nstd209human GRCh38 chr9: 37,817,328-37,826,396 , GRCh37.p13 chr9: 37,817,325-37,826,393 DCAF10
    nsv5968856inversion1nstd209human GRCh38 chr9: 37,821,331-37,824,625 , GRCh37.p13 chr9: 37,821,328-37,824,622 DCAF10
    nsv5926098copy number variation1nstd209human GRCh38 chr9: 37,804,218-37,804,297 , GRCh37.p13 chr9: 37,804,215-37,804,294 DCAF10
    nsv5915117copy number variation1nstd209human GRCh38 chr9: 37,811,791-37,811,998 , GRCh37.p13 chr9: 37,811,788-37,811,995 DCAF10
    nsv5909124copy number variation1nstd209human GRCh38 chr9: 37,817,735-37,821,324 , GRCh37.p13 chr9: 37,817,732-37,821,321 DCAF10
    nsv5708252mobile element insertion2nstd211human GRCh38 chr9: 37,853,519-37,853,519 , GRCh37.p13 chr9: 37,853,516-37,853,516 DCAF10
    nsv5635353insertion1nstd207human GRCh38 chr9: 37,808,524-37,808,524 , GRCh37.p13 chr9: 37,808,521-37,808,521 DCAF10
    nsv5634518insertion2nstd207human GRCh38 chr9: 37,808,748-37,808,748 , GRCh37.p13 chr9: 37,808,745-37,808,745 DCAF10
    nsv5543680insertion1nstd206human GRCh38 chr9: 37,808,748-37,808,748 , GRCh37.p13 chr9: 37,808,745-37,808,745 DCAF10
    nsv5485106copy number variation1nstd206human GRCh38 chr9: 37,814,189-37,818,127 , GRCh37.p13 chr9: 37,814,186-37,818,124 DCAF10
    nsv5481892copy number variation1nstd206human GRCh38 chr9: 37,828,523-37,828,763 , GRCh37.p13 chr9: 37,828,520-37,828,760 DCAF10
    nsv5477382copy number variation1nstd206human GRCh38 chr9: 37,835,319-37,835,466 , GRCh37.p13 chr9: 37,835,316-37,835,463 DCAF10, MRPS10P5
    nsv5401760mobile element insertion1nstd206human GRCh38 chr9: 37,853,519-37,853,556 , GRCh37.p13 chr9: 37,853,516-37,853,553 DCAF10
    nsv5372498translocation1nstd200human GRCh38 chr9: 37,867,748-37,867,748 , GRCh38 chr9: 37,867,837-37,867,837 , GRCh37.p13 chr9: 37,867,834-37,867,834 , GRCh37.p13 chr9: 37,867,745-37,867,745 DCAF10
    nsv5130402mobile element insertion1nstd203human GRCh38 chr9: 37,853,503-37,853,514 , GRCh37.p13 chr9: 37,853,500-37,853,511 DCAF10
    nsv5126299mobile element insertion1nstd203human GRCh38 chr9: 37,853,505-37,853,519 , GRCh37.p13 chr9: 37,853,502-37,853,516 DCAF10
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