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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977361inversion1nstd209human GRCh38 chr7: 5,132,403-5,833,612 , GRCh37.p13 chr7: 5,172,034-5,873,243 , ACTB, 15 more genes
    nsv5974969inversion1nstd209human GRCh37.p13 chr7: 5,533,688-5,535,364 , GRCh38 chr7: 5,494,057-5,495,733 FBXL18, MIR589
    nsv5912393copy number variation1nstd209human GRCh38 chr7: 5,492,442-5,493,930 , GRCh37.p13 chr7: 5,532,073-5,533,561 FBXL18, MIR589
    nsv5847204copy number variation1nstd209human GRCh38 chr7: 5,492,490-5,494,129 , GRCh37.p13 chr7: 5,532,121-5,533,760 FBXL18, MIR589
    nsv5562206sequence alteration1nstd206human GRCh38 chr7: 4,983,711-5,730,820 , GRCh37.p13 chr7: 5,023,342-5,770,451 , FSCN1, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5556597sequence alteration1nstd206human GRCh38 chr7: 5,492,375-5,494,054 , GRCh37.p13 chr7: 5,532,006-5,533,685 FBXL18, MIR589
    nsv5554692sequence alteration1nstd206human GRCh38 chr7: 5,142,858-5,773,733 , GRCh37.p13 chr7: 5,182,489-5,813,364 , FSCN1, 14 more genes
    nsv5464195copy number variation1nstd206human GRCh38 chr7: 5,493,533-5,494,924 , GRCh37.p13 chr7: 5,533,164-5,534,555 MIR589, FBXL18
    nsv5456433copy number variation1nstd206human GRCh38 chr7: 5,492,324-5,494,103 , GRCh37.p13 chr7: 5,531,955-5,533,734 FBXL18, MIR589
    nsv5363638translocation1nstd200human GRCh38 chr7: 5,492,381-5,492,381 , GRCh38 chr7: 5,494,055-5,494,055 , GRCh37.p13 chr7: 5,533,686-5,533,686 , GRCh37.p13 chr7: 5,532,012-5,532,012 MIR589, FBXL18
    nsv5363636translocation1nstd200human GRCh38 chr7: 5,494,054-5,494,054 , GRCh38 chr7: 5,492,374-5,492,374 , GRCh37.p13 chr7: 5,532,005-5,532,005 , GRCh37.p13 chr7: 5,533,685-5,533,685 MIR589, FBXL18
    nsv5235653copy number variation1nstd204human GRCh37.p13 chr7: 5,239,332-5,603,931 , GRCh38.p13 chr7: 5,199,701-5,564,300 ACTB, WIPI2, 7 more genes
    nsv5221353copy number variation1nstd204human GRCh38.p13 chr7: 5,486,801-5,521,600 , GRCh37.p13 chr7: 5,526,432-5,561,231 LOC221946, FBXL18, 1 more genes
    nsv4953290copy number variation1nstd200human GRCh38 chr7: 5,493,828-5,496,918 , GRCh37.p13 chr7: 5,533,459-5,536,549 MIR589, FBXL18
    nsv4949908copy number variation1nstd200human GRCh38 chr7: 5,493,558-5,494,902 , GRCh37.p13 chr7: 5,533,189-5,534,533 MIR589, FBXL18
    nsv4949907copy number variation1nstd200human GRCh38 chr7: 5,484,278-5,507,636 , GRCh37.p13 chr7: 5,523,909-5,547,267 FBXL18, MIR589
    nsv4675817copy number variation1nstd102humanPathogenic GRCh37 chr7: 1,648,373-10,627,513 , GRCh38.p12 chr7: 1,608,737-10,587,886 TTYH3, UNC93B2, 150 more genes
    nsv4662724copy number variation1nstd186human GRCh37 chr7: 5,532,012-5,533,527 , GRCh38.p12 chr7: 5,492,381-5,493,896 FBXL18, MIR589
    nsv4618577copy number variation1nstd183human GRCh37 chr7: 5,532,012-5,533,527 , GRCh38.p12 chr7: 5,492,381-5,493,896 FBXL18, MIR589
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