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Items: 1 to 20 of 266

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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
    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
    nsv6852219copy number variation1nstd229human GRCh38 chr8: 42,171,192-42,213,015 , GRCh37.p13 chr8: 42,028,710-42,070,533 PLAT, AP3M2
    nsv6848591copy number variation1nstd229human GRCh38 chr8: 42,179,797-42,179,827 , GRCh37.p13 chr8: 42,037,315-42,037,345 PLAT
    nsv6845683copy number variation1nstd229human GRCh38 chr8: 42,195,267-42,196,756 , GRCh37.p13 chr8: 42,052,785-42,054,274 PLAT
    nsv6843536copy number variation1nstd229human GRCh38 chr8: 42,202,172-42,208,291 , GRCh37.p13 chr8: 42,059,690-42,065,809 PLAT
    nsv6840873copy number variation1nstd229human GRCh38 chr8: 42,198,050-42,199,248 , GRCh37.p13 chr8: 42,055,568-42,056,766 PLAT
    nsv6840060copy number variation1nstd229human GRCh38 chr8: 42,198,713-42,219,387 , GRCh37.p13 chr8: 42,056,231-42,076,905 PLAT
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6574994inversion1nstd223human GRCh38 chr8: 42,189,412-42,189,853 , GRCh37.p13 chr8: 42,046,930-42,047,371 PLAT
    nsv6431687copy number variation1nstd223human GRCh38 chr8: 42,175,211-42,176,534 , GRCh37.p13 chr8: 42,032,729-42,034,052 PLAT
    nsv6420576copy number variation1nstd223human GRCh38 chr8: 42,202,172-42,208,289 , GRCh37.p13 chr8: 42,059,690-42,065,807 PLAT
    nsv6418320copy number variation1nstd223human GRCh38 chr8: 42,198,713-42,219,387 , GRCh37.p13 chr8: 42,056,231-42,076,905 PLAT
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6245917mobile element insertion1nstd215human GRCh38 chr8: 42,182,388-42,182,388 , GRCh37.p13 chr8: 42,039,906-42,039,906 PLAT
    nsv6136047copy number variation1nstd213human GRCh37 chr8: 41,160,000-42,320,001 , GRCh38.p12 chr8: 41,302,481-42,462,483 SLC20A2, GOLGA7, 27 more genes
    nsv6065860insertion1nstd212human GRCh38 chr8: 42,182,378-42,182,378 , GRCh37.p13 chr8: 42,039,896-42,039,896 PLAT
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