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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093811copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,974,585-91,222,335 , GRCh38.p12 chr10: 89,214,828-89,462,578 SLC16A12-AS1, IFIT1, 10 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6883259copy number variation1nstd229human GRCh38 chr10: 88,909,886-89,428,064 , GRCh37.p13 chr10: 90,669,643-91,187,821 IFIT2, STAMBPL1, 18 more genes
    nsv6883010copy number variation1nstd229human GRCh38 chr10: 89,085,834-89,335,959 , GRCh37.p13 chr10: 90,845,591-91,095,716 IFIT2, CH25H, 6 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637707copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,672,265-91,165,763 , GRCh38.p12 chr10: 88,912,508-89,406,006 IFIT1, IFIT3, 16 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6637182copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,874,051-91,291,188 , GRCh38.p12 chr10: 89,114,294-89,531,431 IFIT5, IFIT6P, 13 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6448408copy number variation1nstd223human GRCh38 chr10: 89,303,365-89,303,769 , GRCh37.p13 chr10: 91,063,122-91,063,526 IFIT2
    nsv6014376copy number variation1nstd212human GRCh38 chr10: 89,302,510-89,302,662 , GRCh37.p13 chr10: 91,062,267-91,062,419 IFIT2
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4743522copy number variation1nstd199human GRCh37 chr10: 91,061,311-91,061,441 , GRCh38.p12 chr10: 89,301,554-89,301,684 LOC105378419, IFIT2
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4682162copy number variation1nstd102humanPathogenic GRCh37 chr10: 90,530,602-91,087,835 , GRCh38.p12 chr10: 88,770,845-89,328,078 MIR4679-2, ACTA2-AS1, 17 more genes
    nsv4455319copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,510,448-91,086,868 , GRCh38.p12 chr10: 88,750,691-89,327,111 PTCD2P2, LIPN, 18 more genes
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