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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137681copy number variation1nstd102humanLikely benign GRCh37 chr9: 135,947,000-135,947,065 , GRCh38 chr9: 133,071,613-133,071,678 CEL
    nsv6112698copy number variation1nstd102humanLikely benign GRCh37 chr9: 135,946,856-135,946,921 , GRCh38 chr9: 133,071,469-133,071,534 CEL
    nsv5918269copy number variation1nstd209human GRCh38 chr9: 133,069,880-133,085,520 , GRCh37.p13 chr9: 135,945,267-135,960,907 CEL, CELP
    nsv5865293copy number variation2nstd209human GRCh38 chr9: 133,063,162-133,068,166 , GRCh37.p13 chr9: 135,938,549-135,943,553 CEL
    nsv5863421copy number variation2nstd209human GRCh38 chr9: 133,060,578-133,061,708 , GRCh37.p13 chr9: 135,935,965-135,937,095 CEL
    nsv5858113copy number variation2nstd209human GRCh38 chr9: 133,068,665-133,081,860 , GRCh37.p13 chr9: 135,944,052-135,957,247 CELP, CEL
    nsv5851229copy number variation3nstd209human GRCh38 chr9: 133,068,666-133,084,217 , GRCh37.p13 chr9: 135,944,053-135,959,604 CEL, CELP
    nsv5595004copy number variation1nstd207human GRCh38 chr9: 133,071,580-133,071,646 , GRCh37.p13 chr9: 135,946,967-135,947,033 CEL
    nsv5591329copy number variation1nstd207human GRCh38 chr9: 133,071,240-133,071,305 , GRCh37.p13 chr9: 135,946,627-135,946,692 CEL
    nsv5590967copy number variation1nstd207human GRCh38 chr9: 133,071,240-133,071,404 , GRCh37.p13 chr9: 135,946,627-135,946,791 CEL
    nsv5487902copy number variation1nstd206human GRCh38 chr9: 133,069,901-133,085,564 , GRCh37.p13 chr9: 135,945,288-135,960,951 CELP, CEL
    nsv5483863copy number variation1nstd206human GRCh38 chr9: 133,060,640-133,081,164 , GRCh37.p13 chr9: 135,936,027-135,956,551 CELP, CEL
    nsv5302333copy number variation1nstd204human GRCh38.p13 chr9: 133,060,374-133,081,384 , GRCh37.p13 chr9: 135,935,761-135,956,771 CEL, CELP
    nsv5256157copy number variation1nstd204human GRCh38.p13 chr9: 133,063,162-133,071,136 , GRCh37.p13 chr9: 135,938,549-135,946,523 CEL
    nsv5255833copy number variation1nstd204human GRCh38.p13 chr9: 133,068,362-133,086,446 , GRCh37.p13 chr9: 135,943,749-135,961,833 CEL, CELP
    nsv5253241copy number variation1nstd204human GRCh38.p13 chr9: 133,060,178-133,063,861 , GRCh37.p13 chr9: 135,935,565-135,939,248 CEL
    nsv5249227copy number variation1nstd204human GRCh38.p13 chr9: 133,061,001-133,071,300 , GRCh37.p13 chr9: 135,936,388-135,946,687 CEL
    nsv5247230copy number variation1nstd204human GRCh38.p13 chr9: 133,071,601-133,082,300 , GRCh37.p13 chr9: 135,946,988-135,957,687 CEL, CELP
    nsv5245914copy number variation1nstd204human GRCh38.p13 chr9: 133,061,101-133,081,200 , GRCh37.p13 chr9: 135,936,488-135,956,587 CEL, CELP
    nsv5242481copy number variation1nstd204human GRCh38.p13 chr9: 133,070,641-133,083,947 , GRCh37.p13 chr9: 135,946,028-135,959,334 CEL, CELP
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