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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
    nsv7072730inversion1nstd229human GRCh38 chr8: 42,723,314-42,728,037 , GRCh37.p13 chr8: 42,578,457-42,583,180 CHRNB3, RPL7L1P17
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv6856380copy number variation1nstd229human GRCh38 chr8: 42,708,101-42,836,600 , GRCh37.p13 chr8: 42,563,244-42,691,743 CHRNA6, CHRNB3, 2 more genes
    nsv6855900copy number variation1nstd229human GRCh38 chr8: 42,710,771-42,719,896 , GRCh37.p13 chr8: 42,565,914-42,575,039 CHRNB3
    nsv6855852copy number variation1nstd229human GRCh38 chr8: 42,736,201-42,736,403 , GRCh37.p13 chr8: 42,591,344-42,591,546 CHRNB3
    nsv6854193copy number variation1nstd229human GRCh38 chr8: 42,567,101-42,843,300 , GRCh37.p13 chr8: 42,422,244-42,698,443 LOC105379396, THAP1, 3 more genes
    nsv6852190copy number variation1nstd229human GRCh38 chr8: 42,714,301-42,718,400 , GRCh37.p13 chr8: 42,569,444-42,573,543 CHRNB3
    nsv6851394copy number variation1nstd229human GRCh38 chr8: 42,716,001-42,739,400 , GRCh37.p13 chr8: 42,571,144-42,594,543 RPL7L1P17, CHRNB3
    nsv6848652copy number variation1nstd229human GRCh38 chr8: 42,714,201-42,719,500 , GRCh37.p13 chr8: 42,569,344-42,574,643 CHRNB3
    nsv6848352copy number variation1nstd229human GRCh38 chr8: 42,717,301-42,735,300 , GRCh37.p13 chr8: 42,572,444-42,590,443 CHRNB3, RPL7L1P17
    nsv6843418copy number variation1nstd229human GRCh38 chr8: 42,712,901-42,740,700 , GRCh37.p13 chr8: 42,568,044-42,595,843 RPL7L1P17, CHRNB3
    nsv6842044copy number variation1nstd229human GRCh38 chr8: 42,718,445-42,735,265 , GRCh37.p13 chr8: 42,573,588-42,590,408 RPL7L1P17, CHRNB3
    nsv6840806copy number variation1nstd229human GRCh38 chr8: 42,700,335-42,708,952 , GRCh37.p13 chr8: 42,555,478-42,564,095 CHRNB3, LOC105379396
    nsv6838430copy number variation1nstd229human GRCh38 chr8: 42,718,301-42,735,300 , GRCh37.p13 chr8: 42,573,444-42,590,443 RPL7L1P17, CHRNB3
    nsv6637131copy number variation1nstd102humanPathogenic GRCh37 chr8: 42,303,398-43,002,481 , GRCh38.p12 chr8: 42,445,880-43,147,338 RNU1-124P, LOC105379396, 13 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6633052copy number variation1nstd224human GRCh37 chr8: 42,572,589-42,585,694 , GRCh38.p12 chr8: 42,717,446-42,730,551 RPL7L1P17, CHRNB3
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