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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074187inversion1nstd229human GRCh38 chr9: 19,053,656-19,053,684 , GRCh37.p13 chr9: 19,053,654-19,053,682 HAUS6
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7068284inversion1nstd229human GRCh38 chr9: 19,080,709-19,084,832 , GRCh37.p13 chr9: 19,080,707-19,084,830 HAUS6
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6877491copy number variation1nstd229human GRCh38 chr9: 19,051,325-19,081,825 , GRCh37.p13 chr9: 19,051,323-19,081,823 HAUS6, SCARNA8, 2 more genes
    nsv6877415copy number variation1nstd229human GRCh38 chr9: 18,863,175-19,659,789 , GRCh37.p13 chr9: 18,863,173-19,659,787 ACER2, ADAMTSL1, 15 more genes
    nsv6876774copy number variation1nstd229human GRCh38 chr9: 18,968,809-19,051,746 , GRCh37.p13 chr9: 18,968,807-19,051,744 HAUS6, SAXO1, 2 more genes
    nsv6874370copy number variation1nstd229human GRCh38 chr9: 19,077,797-19,550,661 , GRCh37.p13 chr9: 19,077,795-19,550,659 RPS6P10, MAP1LC3BP1, 8 more genes
    nsv6872144copy number variation1nstd229human GRCh38 chr9: 19,063,888-19,089,861 , GRCh37.p13 chr9: 19,063,886-19,089,859 SCARNA8, HAUS6, 1 more genes
    nsv6872097copy number variation1nstd229human GRCh38 chr9: 19,064,872-19,076,376 , GRCh37.p13 chr9: 19,064,870-19,076,374 HAUS6, RNU6-264P
    nsv6871425copy number variation1nstd229human GRCh38 chr9: 19,085,092-19,085,528 , GRCh37.p13 chr9: 19,085,090-19,085,526 HAUS6
    nsv6867768copy number variation1nstd229human GRCh38 chr9: 17,165,352-20,022,245 , GRCh37.p13 chr9: 17,165,350-20,022,243 SH3GL2, SLC24A2, 31 more genes
    nsv6863740copy number variation1nstd229human GRCh38 chr9: 19,089,211-19,375,587 , GRCh37.p13 chr9: 19,089,209-19,375,585 RPS6, RPS6P10, 3 more genes
    nsv6863217copy number variation1nstd229human GRCh38 chr9: 19,081,514-19,084,708 , GRCh37.p13 chr9: 19,081,512-19,084,706 HAUS6
    nsv6861485copy number variation1nstd229human GRCh38 chr9: 19,080,401-19,156,700 , GRCh37.p13 chr9: 19,080,399-19,156,698 HAUS6, PLIN2
    nsv6861042copy number variation1nstd229human GRCh38 chr9: 18,675,227-19,114,754 , GRCh37.p13 chr9: 18,675,225-19,114,752 LOC102724102, RRAGA, 9 more genes
    nsv6860277copy number variation1nstd229human GRCh38 chr9: 18,994,780-19,150,586 , GRCh37.p13 chr9: 18,994,778-19,150,584 RRAGA, SCARNA8, 5 more genes
    nsv6859250copy number variation1nstd229human GRCh38 chr9: 19,061,561-19,079,165 , GRCh37.p13 chr9: 19,061,559-19,079,163 RNU6-264P, SCARNA8, 1 more genes
    nsv6637746copy number variation1nstd102humanUncertain significance GRCh37 chr9: 18,960,334-19,191,447 , GRCh38.p12 chr9: 18,960,336-19,191,449 RNU6-264P, RRAGA, 5 more genes
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