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Items: 1 to 20 of 154

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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
    nsv7065639inversion1nstd229human GRCh38 chr8: 40,079,981-42,715,940 , GRCh37.p13 chr8: 39,937,500-42,571,083 LOC105379390, RPL17P30, 44 more genes
    nsv6857693copy number variation1nstd229human GRCh38 chr8: 39,767,660-40,175,274 , GRCh37.p13 chr8: 39,625,179-40,032,793 LOC100420480, ADAM2, 6 more genes
    nsv6850956copy number variation1nstd229human GRCh38 chr8: 40,152,053-40,152,792 , GRCh37.p13 chr8: 40,009,572-40,010,311 LOC105379385, TCIM
    nsv6839650copy number variation1nstd229human GRCh38 chr8: 38,572,201-41,442,522 , GRCh37.p13 chr8: 38,429,719-41,300,041 RPL3P10, SNORD65B, 35 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6313822copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,430,146-41,294,984 , GRCh38.p12 chr8: 38,572,628-41,437,465 RNU6-895P, ADAM9, 35 more genes
    nsv6137286copy number variation1nstd213human GRCh37 chr8: 39,480,000-40,640,001 , GRCh38.p12 chr8: 39,622,481-40,782,482 LINC02866, LOC107986938, 11 more genes
    nsv6137284copy number variation1nstd213human GRCh37 chr8: 39,010,000-41,480,001 , GRCh38.p12 chr8: 39,152,481-41,622,482 ADAM3A, ADAM2, 32 more genes
    nsv6136044copy number variation1nstd213human GRCh37 chr8: 39,020,000-41,480,001 , GRCh38.p12 chr8: 39,162,481-41,622,482 ADAM3A, ADAM2, 31 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4675652copy number variation1nstd102humanUncertain significance GRCh37 chr8: 39,856,646-40,562,257 , GRCh38.p12 chr8: 39,999,127-40,704,738 ZMAT4, LOC107986938, 6 more genes
    nsv4616745copy number variation1nstd183human GRCh37 chr8: 40,012,143-40,013,033 , GRCh38.p12 chr8: 40,154,624-40,155,514 TCIM, LOC105379385
    nsv4609634copy number variation1nstd183human GRCh37 chr8: 40,003,410-40,012,294 , GRCh38.p12 chr8: 40,145,891-40,154,775 TCIM, LOC105379385
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456199copy number variation1nstd102humanUncertain significance GRCh37 chr8: 36,094,421-43,822,214 , GRCh38.p12 chr8: 36,236,903-43,967,071 AFG3L2P1, BRF2, 136 more genes
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