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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
    nsv7098695delins1nstd102humanUncertain significance GRCh37 chr17: 45,016,105-45,016,110 , GRCh38 chr17: 46,938,739-46,938,744 GOSR2, LRRC37A2
    nsv7073784inversion1nstd229human GRCh38 chr17: 46,956,129-46,962,696 , GRCh37.p13 chr17: 45,033,495-45,040,062 GOSR2, LRRC37A2
    nsv7068560inversion1nstd229human GRCh38 chr17: 46,952,946-46,955,814 , GRCh37.p13 chr17: 45,030,312-45,033,180 LRRC37A2, GOSR2
    nsv6995067copy number variation1nstd229human GRCh38 chr17: 46,931,846-46,931,987 , GRCh37.p13 chr17: 45,009,212-45,009,353 GOSR2, 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
    nsv6978762copy number variation1nstd229human GRCh38 chr17: 46,949,054-46,949,137 , GRCh37.p13 chr17: 45,026,420-45,026,503 LRRC37A2, GOSR2
    nsv6586175inversion1nstd223human GRCh38 chr17: 46,946,296-46,947,789 , GRCh37.p13 chr17: 45,023,662-45,025,155 GOSR2, LRRC37A2
    nsv6522493copy number variation1nstd223human GRCh38 chr17: 46,970,333-46,974,459 , GRCh37.p13 chr17: 45,047,699-45,051,825 MIR5089, LRRC37A2, 1 more genes
    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
    nsv6310389copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 44,845,686-45,016,126 , GRCh38.p12 chr17: 46,768,320-46,938,760 , GRCh38.p12 chr17|NT_187663.1: 1,287,733-1,423,190 WNT3, WNT9B, 6 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
    nsv6250823mobile element insertion1nstd215human GRCh38 chr17: 46,975,013-46,975,013 , GRCh37.p13 chr17: 45,052,379-45,052,379 GOSR2, LRRC37A2
    nsv6250822mobile element insertion1nstd215human GRCh38 chr17: 46,929,904-46,929,904 , GRCh37.p13 chr17: 45,007,270-45,007,270 LRRC37A2, GOSR2
    nsv6250821mobile element insertion1nstd215human GRCh38 chr17: 46,927,840-46,927,840 , GRCh37.p13 chr17: 45,005,206-45,005,206 LRRC37A2, GOSR2
    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
    nsv6032420copy number variation1nstd212human GRCh38 chr17: 46,945,542-46,947,456 , GRCh37.p13 chr17: 45,022,908-45,024,822 LRRC37A2, GOSR2
    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
    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
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