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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5943206copy number variation1nstd209human GRCh38 chr18: 26,205,242-26,208,976 , GRCh37.p13 chr18: 23,785,206-23,788,940 NPM1P2
    nsv5939751copy number variation1nstd209human GRCh38 chr18: 26,195,350-26,213,666 , GRCh37.p13 chr18: 23,775,314-23,793,630 NPM1P2
    nsv5877031copy number variation1nstd209human GRCh38 chr18: 26,195,602-26,204,485 , GRCh37.p13 chr18: 23,775,566-23,784,449 NPM1P2
    nsv5875625copy number variation1nstd209human GRCh38 chr18: 26,205,061-26,208,824 , GRCh37.p13 chr18: 23,785,025-23,788,788 NPM1P2
    nsv5531377copy number variation1nstd206human GRCh38 chr18: 26,205,242-26,208,981 , GRCh37.p13 chr18: 23,785,206-23,788,945 NPM1P2
    nsv5524763copy number variation1nstd206human GRCh38 chr18: 26,195,340-26,213,696 , GRCh37.p13 chr18: 23,775,304-23,793,660 NPM1P2
    nsv5024025copy number variation1nstd200human GRCh38 chr18: 26,195,349-26,213,688 , GRCh37.p13 chr18: 23,775,313-23,793,652 NPM1P2
    nsv4854591copy number variation1nstd200human GRCh37 chr18: 23,775,311-23,793,654 , GRCh38.p12 chr18: 26,195,347-26,213,690 NPM1P2
    nsv4729865copy number variation1nstd102humanUncertain significance GRCh37 chr18: 23,586,307-25,193,192 , GRCh38.p12 chr18: 26,006,343-27,613,228 ATP6V1E1P2, SINHCAFP1, 29 more genes
    nsv4676233copy number variation1nstd102humanPathogenic GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790 DHFRP1, CLUHP6, 116 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4422211copy number variation1nstd174human GRCh37 chr18: 23,777,843-23,791,563 , GRCh38.p12 chr18: 26,197,879-26,211,599 NPM1P2
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4272119copy number variation1nstd166human GRCh37.p13 chr18: 23,746,004-23,931,195 , GRCh38.p12 chr18: 26,166,040-26,351,231 NPM1P2, TAF4B, 4 more genes
    nsv4256195copy number variation1nstd166human GRCh37.p13 chr18: 23,785,206-23,788,945 , GRCh38.p12 chr18: 26,205,242-26,208,981 NPM1P2
    nsv4255867copy number variation1nstd166human GRCh37.p13 chr18: 23,775,377-23,793,651 , GRCh38.p12 chr18: 26,195,413-26,213,687 NPM1P2
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
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