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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141974insertion1nstd232human GRCh37.p13 chr9: 15,465,578-15,465,578 , GRCh38.p12 chr9: 15,465,580-15,465,580 SNAPC3, PSIP1
    nsv7072719inversion1nstd229human GRCh38 chr9: 14,792,079-19,156,478 , GRCh37.p13 chr9: 14,792,077-19,156,476 RN7SL98P, RRAGA, 49 more genes
    nsv7069362inversion1nstd229human GRCh38 chr9: 15,508,211-15,509,478 , GRCh37.p13 chr9: 15,508,209-15,509,476 PSIP1
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6875307copy number variation1nstd229human GRCh38 chr9: 15,474,466-15,474,872 , GRCh37.p13 chr9: 15,474,464-15,474,870 PSIP1
    nsv6870715copy number variation1nstd229human GRCh38 chr9: 15,495,847-15,501,005 , GRCh37.p13 chr9: 15,495,845-15,501,003 PSIP1
    nsv6869373copy number variation1nstd229human GRCh38 chr9: 15,398,031-15,518,460 , GRCh37.p13 chr9: 15,398,029-15,518,458 PSIP1, RNU6-319P, 1 more genes
    nsv6868976copy number variation1nstd229human GRCh38 chr9: 15,246,386-15,506,731 , GRCh37.p13 chr9: 15,246,384-15,506,729 SNAPC3, RNU6-319P, 3 more genes
    nsv6868114copy number variation1nstd229human GRCh38 chr9: 15,401,639-15,462,924 , GRCh37.p13 chr9: 15,401,637-15,462,922 SNAPC3, PSIP1, 1 more genes
    nsv6867761copy number variation1nstd229human GRCh38 chr9: 15,484,275-15,487,949 , GRCh37.p13 chr9: 15,484,273-15,487,947 PSIP1
    nsv6864755copy number variation1nstd229human GRCh38 chr9: 15,460,102-15,462,088 , GRCh37.p13 chr9: 15,460,100-15,462,086 SNAPC3, PSIP1
    nsv6863511copy number variation1nstd229human GRCh38 chr9: 15,455,321-15,483,605 , GRCh37.p13 chr9: 15,455,319-15,483,603 PSIP1, SNAPC3
    nsv6863269copy number variation1nstd229human GRCh38 chr9: 15,507,263-15,507,763 , GRCh37.p13 chr9: 15,507,261-15,507,761 PSIP1
    nsv6862750copy number variation1nstd229human GRCh38 chr9: 15,492,616-15,496,938 , GRCh37.p13 chr9: 15,492,614-15,496,936 PSIP1
    nsv6860127copy number variation1nstd229human GRCh38 chr9: 15,491,847-15,505,153 , GRCh37.p13 chr9: 15,491,845-15,505,151 PSIP1
    nsv6638046copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,241,646-15,504,917 , GRCh38.p12 chr9: 15,241,648-15,504,919 TTC39B, RPL7P33, 3 more genes
    nsv6637721copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,337,857-15,547,347 , GRCh38.p12 chr9: 15,337,859-15,547,349 PSIP1, RNU6-246P, 6 more genes
    nsv6637417copy number variation1nstd102humanUncertain significance GRCh37 chr9: 15,328,600-20,821,644 , GRCh38.p12 chr9: 15,328,602-20,821,645 LSM1P1, RRAGA, 60 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
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