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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7143301copy number variation1nstd232human GRCh37.p13 chr8: 27,366,436-27,366,556 , GRCh38.p12 chr8: 27,508,919-27,509,039 EPHX2
    nsv7073126inversion1nstd229human GRCh38 chr8: 27,092,704-27,554,548 , GRCh37.p13 chr8: 26,950,221-27,412,065 STMN4, LOC105379340, 5 more genes
    nsv7069162inversion1nstd229human GRCh38 chr8: 27,541,022-27,544,703 , GRCh37.p13 chr8: 27,398,539-27,402,220 EPHX2
    nsv7061563inversion1nstd229human GRCh38 chr8: 27,492,341-29,312,113 , GRCh37.p13 chr8: 27,349,858-29,169,630 LOC100130612, HMBOX1, 37 more genes
    nsv6856184copy number variation1nstd229human GRCh38 chr8: 27,505,101-27,506,500 , GRCh37.p13 chr8: 27,362,618-27,364,017 EPHX2
    nsv6856053copy number variation1nstd229human GRCh38 chr8: 27,586,980-27,592,594 , GRCh37.p13 chr8: 27,444,497-27,450,111 EPHX2, GULOP
    nsv6855501copy number variation1nstd229human GRCh38 chr8: 27,507,322-27,517,480 , GRCh37.p13 chr8: 27,364,839-27,374,997 EPHX2
    nsv6852249copy number variation1nstd229human GRCh38 chr8: 27,427,694-27,580,324 , GRCh37.p13 chr8: 27,285,211-27,437,841 PTK2B, CHRNA2, 3 more genes
    nsv6851187copy number variation1nstd229human GRCh38 chr8: 27,493,901-27,498,000 , GRCh37.p13 chr8: 27,351,418-27,355,517 EPHX2
    nsv6849386copy number variation1nstd229human GRCh38 chr8: 27,579,569-27,596,598 , GRCh37.p13 chr8: 27,437,086-27,454,115 EPHX2, GULOP, 1 more genes
    nsv6847733copy number variation1nstd229human GRCh38 chr8: 27,536,121-27,540,746 , GRCh37.p13 chr8: 27,393,638-27,398,263 EPHX2
    nsv6846940copy number variation1nstd229human GRCh38 chr8: 27,523,483-27,533,660 , GRCh37.p13 chr8: 27,381,000-27,391,177 EPHX2
    nsv6845912copy number variation1nstd229human GRCh38 chr8: 27,467,384-27,493,458 , GRCh37.p13 chr8: 27,324,901-27,350,975 EPHX2, CHRNA2
    nsv6844965copy number variation1nstd229human GRCh38 chr8: 27,494,547-27,499,725 , GRCh37.p13 chr8: 27,352,064-27,357,242 EPHX2
    nsv6843669copy number variation1nstd229human GRCh38 chr8: 27,518,765-27,523,105 , GRCh37.p13 chr8: 27,376,282-27,380,622 EPHX2
    nsv6843162copy number variation1nstd229human GRCh38 chr8: 27,484,003-27,506,751 , GRCh37.p13 chr8: 27,341,520-27,364,268 EPHX2
    nsv6842914copy number variation1nstd229human GRCh38 chr8: 27,559,456-27,565,603 , GRCh37.p13 chr8: 27,416,973-27,423,120 EPHX2
    nsv6842629copy number variation1nstd229human GRCh38 chr8: 27,506,775-27,547,197 , GRCh37.p13 chr8: 27,364,292-27,404,714 EPHX2
    nsv6841827copy number variation1nstd229human GRCh38 chr8: 27,473,687-27,506,756 , GRCh37.p13 chr8: 27,331,204-27,364,273 EPHX2, CHRNA2
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