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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7097903copy number variation1nstd102humanUncertain significance GRCh37 chr8: 41,518,984-42,698,237 , GRCh38.p12 chr8: 41,661,466-42,843,094 DKK4, KAT6A, 22 more genes
    nsv7097662copy number variation2nstd102humanUncertain significance GRCh37 chr8: 41,518,984-43,054,712 , GRCh38.p12 chr8: 41,661,466-43,199,569 LOC101059972, IKBKB-DT, 31 more genes
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv6856819copy number variation1nstd229human GRCh38 chr8: 42,329,701-42,336,400 , GRCh37.p13 chr8: 42,187,219-42,193,918 IKBKB
    nsv6855899copy number variation1nstd229human GRCh38 chr8: 42,298,084-42,300,114 , GRCh37.p13 chr8: 42,155,602-42,157,632 IKBKB, LOC105379395
    nsv6853440copy number variation1nstd229human GRCh38 chr8: 42,187,401-42,301,200 , GRCh37.p13 chr8: 42,044,919-42,158,718 LOC105379395, IKBKB-DT, 2 more genes
    nsv6848526copy number variation1nstd229human GRCh38 chr8: 42,272,809-42,276,104 , GRCh37.p13 chr8: 42,130,327-42,133,622 IKBKB
    nsv6841727copy number variation1nstd229human GRCh38 chr8: 42,332,975-42,336,835 , GRCh37.p13 chr8: 42,190,493-42,194,353 IKBKB, POLB
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6560543inversion1nstd223human GRCh38 chr8: 42,311,498-42,312,075 , GRCh37.p13 chr8: 42,169,016-42,169,593 IKBKB
    nsv6423320copy number variation1nstd223human GRCh38 chr8: 42,290,337-42,290,374 , GRCh37.p13 chr8: 42,147,855-42,147,892 IKBKB
    nsv6416137copy number variation1nstd223human GRCh38 chr8: 42,332,950-42,336,834 , GRCh37.p13 chr8: 42,190,468-42,194,352 POLB, IKBKB
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6313701copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,162,574-48,757,095 , GRCh38.p12 chr8: 42,305,056-47,844,534 RNU1-124P, LOC728587, 66 more genes
    nsv6312910copy number variation1nstd102humanUncertain significance GRCh37 chr8: 42,129,619-42,188,497 , GRCh38.p12 chr8: 42,272,101-42,330,979 LOC105379395, IKBKB
    nsv6283533insertion1nstd214human GRCh38 chr8: 42,275,228-42,275,228 , GRCh37.p13 chr8: 42,132,746-42,132,746 IKBKB
    nsv6142836copy number variation1nstd206human GRCh38 chr8: 42,275,228-42,275,286 , GRCh37.p13 chr8: 42,132,746-42,132,804 IKBKB
    nsv6136885translocation1nstd213human GRCh38.p12 chr8: 15,731,051-15,731,051 , GRCh38.p12 chr8: 42,332,346-42,332,346 , GRCh37 chr8: 42,189,864-42,189,864 , GRCh37 chr8: 15,588,560-15,588,560 IKBKB, TUSC3
    nsv6136049copy number variation1nstd213human GRCh37 chr8: 42,190,000-43,790,001 , GRCh38.p12 chr8: 42,332,482-43,934,858 IKBKB, SLC20A2, 29 more genes
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