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Items: 1 to 20 of 197

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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
    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
    nsv6850476copy number variation1nstd229human GRCh38 chr8: 39,914,069-39,919,878 , GRCh37.p13 chr8: 39,771,588-39,777,397 IDO1
    nsv6849116copy number variation1nstd229human GRCh38 chr8: 39,849,968-39,996,660 , GRCh37.p13 chr8: 39,707,487-39,854,179 IDO1, IDO2, 2 more genes
    nsv6842133copy number variation1nstd229human GRCh38 chr8: 39,913,732-39,913,930 , GRCh37.p13 chr8: 39,771,251-39,771,449 IDO1
    nsv6839785copy number variation1nstd229human GRCh38 chr8: 39,911,973-39,918,694 , GRCh37.p13 chr8: 39,769,492-39,776,213 IDO1
    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
    nsv6839103copy number variation1nstd229human GRCh38 chr8: 39,904,954-39,912,240 , GRCh37.p13 chr8: 39,762,473-39,769,759 IDO1
    nsv6838853copy number variation1nstd229human GRCh38 chr8: 39,923,397-39,935,460 , GRCh37.p13 chr8: 39,780,916-39,792,979 LOC100420480, IDO2, 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
    nsv6632982copy number variation1nstd224human GRCh37 chr8: 38,762,056-39,892,501 , GRCh38.p12 chr8: 38,904,538-40,034,982 , GRCh38.p12 chr8|NT_187577.1: 1-624,492 ADAM9, SNORD38D, 15 more genes
    nsv6567703inversion1nstd223human GRCh38 chr8: 39,914,783-39,916,002 , GRCh37.p13 chr8: 39,772,302-39,773,521 IDO1
    nsv6435465copy number variation1nstd223human GRCh38 chr8: 39,911,973-39,918,691 , GRCh37.p13 chr8: 39,769,492-39,776,210 IDO1
    nsv6432883copy number variation1nstd223human GRCh38 chr8: 39,917,160-39,923,064 , GRCh37.p13 chr8: 39,774,679-39,780,583 IDO1
    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
    nsv6137285copy number variation1nstd213human GRCh37 chr8: 39,170,000-39,870,001 , GRCh38.p12 chr8: 39,312,481-40,012,482 , GRCh38.p12 chr8|NT_187577.1: 218,186-624,492 ADAM3A, ADAM2, 7 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
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