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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5481817copy number variation1nstd206human GRCh38 chr8: 18,387,207-18,387,274 , GRCh37.p13 chr8: 18,244,717-18,244,784 NAT2
    nsv5379091translocation1nstd200human GRCh38 chr8: 18,397,712-18,397,712 , GRCh38 chr8: 18,395,843-18,395,843 , GRCh37.p13 chr8: 18,253,353-18,253,353 , GRCh37.p13 chr8: 18,255,222-18,255,222 NAT2
    nsv5379090translocation1nstd200human GRCh38 chr8: 18,397,705-18,397,705 , GRCh38 chr8: 18,395,741-18,395,741 , GRCh37.p13 chr8: 18,253,251-18,253,251 , GRCh37.p13 chr8: 18,255,215-18,255,215 NAT2
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4954218copy number variation1nstd200human GRCh38 chr8: 18,342,407-18,393,983 , GRCh37.p13 chr8: 18,199,916-18,251,493 NAT2, RPL10AP11, 1 more genes
    nsv4954217copy number variation1nstd200human GRCh38 chr8: 18,314,052-18,387,433 , GRCh37.p13 chr8: 18,171,561-18,244,943 NAT2, RPL10AP11, 1 more genes
    nsv4954212copy number variation1nstd200human GRCh38 chr8: 18,067,631-18,560,171 , GRCh37.p13 chr8: 17,925,140-18,417,681 ASAH1-AS1, NAT1, 9 more genes
    nsv4825657copy number variation1nstd200human GRCh37 chr8: 18,199,916-18,251,493 , GRCh38.p12 chr8: 18,342,407-18,393,983 NAT2, RPL10AP11, 1 more genes
    nsv4729680copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,878,070-18,529,463 , GRCh38.p12 chr8: 18,020,561-18,671,953 NATP, MRPS18CP3, 10 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4614753copy number variation1nstd183human GRCh37 chr8: 18,076,411-18,266,307 , GRCh38.p12 chr8: 18,218,902-18,408,797 NAT2, NAT1, 3 more genes
    nsv4607108copy number variation1nstd183human GRCh37 chr8: 18,183,470-18,262,546 , GRCh38.p12 chr8: 18,325,961-18,405,036 NATP, RPL10AP11, 1 more genes
    nsv4606277copy number variation1nstd183human GRCh37 chr8: 18,178,457-18,258,787 , GRCh38.p12 chr8: 18,320,948-18,401,277 NATP, NAT2, 1 more genes
    nsv4550401insertion1nstd166human GRCh37.p13 chr8: 18,255,214-18,255,214 , GRCh38.p12 chr8: 18,397,704-18,397,704 NAT2
    nsv4524124copy number variation1nstd166human GRCh37.p13 chr8: 18,244,717-18,244,784 , GRCh38.p12 chr8: 18,387,207-18,387,274 NAT2
    nsv4457323copy number variation1nstd102humanUncertain significance GRCh37 chr8: 17,575,940-18,443,131 , GRCh38.p12 chr8: 17,718,431-18,585,621 ASAH1-AS1, FGL1, 14 more genes
    nsv4388758copy number variation1nstd171human GRCh37 chr8: 18,245,335-18,245,369 , GRCh38.p12 chr8: 18,387,825-18,387,859 NAT2
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4343252sequence alteration1nstd166human GRCh37.p13 chr8: 18,253,250-18,255,227 , GRCh38.p12 chr8: 18,395,740-18,397,717 NAT2
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