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Items: 1 to 20 of 295

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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
    nsv6853793copy number variation1nstd229human GRCh38 chr8: 41,292,276-41,294,528 , GRCh37.p13 chr8: 41,149,795-41,152,047 SFRP1
    nsv6853572copy number variation1nstd229human GRCh38 chr8: 41,237,401-41,343,100 , GRCh37.p13 chr8: 41,094,920-41,200,619 SFRP1, RPS29P2, 2 more genes
    nsv6851860copy number variation1nstd229human GRCh38 chr8: 41,293,376-41,305,992 , GRCh37.p13 chr8: 41,150,895-41,163,511 SFRP1, RNU6-895P
    nsv6850449copy number variation1nstd229human GRCh38 chr8: 41,163,697-41,568,923 , GRCh37.p13 chr8: 41,021,216-41,426,442 SFRP1, LOC105379771, 9 more genes
    nsv6849708copy number variation1nstd229human GRCh38 chr8: 41,286,010-41,297,295 , GRCh37.p13 chr8: 41,143,529-41,154,814 SFRP1, RNU6-895P
    nsv6847987copy number variation1nstd229human GRCh38 chr8: 41,276,936-41,281,214 , GRCh37.p13 chr8: 41,134,455-41,138,733 SFRP1
    nsv6846093copy number variation1nstd229human GRCh38 chr8: 41,297,146-41,355,317 , GRCh37.p13 chr8: 41,154,665-41,212,836 SFRP1, RNU6-895P
    nsv6846011copy number variation1nstd229human GRCh38 chr8: 40,859,599-41,864,333 , GRCh37.p13 chr8: 40,717,118-41,721,851 MIR548AO, LOC105379392, 20 more genes
    nsv6841338copy number variation1nstd229human GRCh38 chr8: 41,304,818-41,304,928 , GRCh37.p13 chr8: 41,162,337-41,162,447 SFRP1
    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
    nsv6839154copy number variation1nstd229human GRCh38 chr8: 41,267,301-41,269,900 , GRCh37.p13 chr8: 41,124,820-41,127,419 RPS29P2, MIR548AO, 1 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632987copy number variation1nstd224human GRCh37 chr8: 41,161,759-41,615,138 , GRCh38.p12 chr8: 41,304,240-41,757,620 ANK1, NKX6-3, 10 more genes
    nsv6430464copy number variation1nstd223human GRCh38 chr8: 41,150,220-41,456,698 , GRCh37.p13 chr8: 41,007,739-41,314,217 RNU6-895P, MIR548AO, 5 more genes
    nsv6421486copy number variation1nstd223human GRCh38 chr8: 41,262,302-41,410,732 , GRCh37.p13 chr8: 41,119,821-41,268,251 RPS29P2, MIR548AO, 2 more genes
    nsv6416383copy number variation1nstd223human GRCh38 chr8: 41,307,801-41,310,100 , GRCh37.p13 chr8: 41,165,320-41,167,619 SFRP1
    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
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