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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137094copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 44,949,883-46,507,482 , GRCh38.p12 chr17: 46,872,517-48,430,120 CDC27, ITGB3, 49 more genes
    nsv6992695copy number variation1nstd229human GRCh38 chr17: 46,976,179-46,976,783 , GRCh37.p13 chr17: 45,053,545-45,054,149 RPRML, LRRC37A2
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6525096copy number variation1nstd223human GRCh38 chr17: 46,978,001-46,979,900 , GRCh37.p13 chr17: 45,055,367-45,057,266 LRRC37A2, RPRML
    nsv6524158copy number variation1nstd223human GRCh38 chr17: 46,976,179-46,976,783 , GRCh37.p13 chr17: 45,053,545-45,054,149 RPRML, LRRC37A2
    nsv6497344copy number variation1nstd223human GRCh38 chr17: 46,098,250-47,084,546 , GRCh37.p13 chr17: 44,175,616-45,161,912 ARL17A, MIR5089, 27 more genes
    nsv6291493copy number variation1nstd102humanUncertain significance GRCh37 chr17: 45,044,413-45,170,820 , GRCh38.p12 chr17: 46,967,047-47,093,454 RPRML, LRRC37A2, 5 more genes
    nsv6133312copy number variation1nstd213human GRCh37 chr17: 44,650,000-45,170,001 , GRCh38.p12 chr17: 46,572,634-47,092,635 , GRCh38.p12 chr17|NT_187663.1: 1,092,338-1,423,190 NSF, WNT3, 15 more genes
    nsv6029850copy number variation1nstd212human GRCh38 chr17: 46,974,500-46,976,280 , GRCh37.p13 chr17: 45,051,866-45,053,646 GOSR2, RPRML, 1 more genes
    nsv5944572copy number variation1nstd209human GRCh38 chr17: 46,210,492-47,098,378 , GRCh37.p13 chr17: 44,287,858-45,175,744 , KANSL1, 26 more genes
    nsv5942396copy number variation1nstd209human GRCh38 chr17: 46,976,179-46,976,782 , GRCh37.p13 chr17: 45,053,545-45,054,148 RPRML, LRRC37A2
    nsv5936729copy number variation1nstd209human GRCh38 chr17: 46,974,475-46,976,272 , GRCh37.p13 chr17: 45,051,841-45,053,638 GOSR2, RPRML, 1 more genes
    nsv5882207copy number variation1nstd209human GRCh38 chr17: 46,974,260-46,976,355 , GRCh37.p13 chr17: 45,051,626-45,053,721 LRRC37A2, GOSR2, 1 more genes
    nsv5598461copy number variation1nstd207human GRCh38 chr17: 46,976,179-46,976,782 , GRCh37.p13 chr17: 45,053,545-45,054,148 LRRC37A2, RPRML
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5532697copy number variation1nstd206human GRCh38 chr17: 46,974,457-46,976,321 , GRCh37.p13 chr17: 45,051,823-45,053,687 GOSR2, RPRML, 1 more genes
    nsv5529674copy number variation1nstd206human GRCh38 chr17: 46,976,179-46,976,783 , GRCh37.p13 chr17: 45,053,545-45,054,149 RPRML, LRRC37A2
    nsv5358904translocation1nstd200human GRCh38 chr17: 46,976,783-46,976,783 , GRCh38 chr17: 46,976,179-46,976,179 , GRCh37.p13 chr17: 45,053,545-45,053,545 , GRCh37.p13 chr17: 45,054,149-45,054,149 RPRML, LRRC37A2
    nsv5339825translocation1nstd200human GRCh37 chr17: 45,053,545-45,053,545 , GRCh37 chr17: 45,054,149-45,054,149 , GRCh38.p12 chr17: 46,976,783-46,976,783 , GRCh38.p12 chr17: 46,976,179-46,976,179 RPRML, LRRC37A2
    nsv5328790copy number variation1nstd204human GRCh37.p13 chr17: 45,051,874-45,053,653 , GRCh38.p13 chr17: 46,974,508-46,976,287 GOSR2, RPRML, 1 more genes
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