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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974932inversion1nstd209human GRCh38 chr8: 70,050,413-70,058,706 , GRCh37.p13 chr8: 70,962,648-70,970,941 PRDM14
    nsv5854773copy number variation1nstd209human GRCh38 chr8: 70,048,842-70,050,441 , GRCh37.p13 chr8: 70,961,077-70,962,676 PRDM14
    nsv5483115copy number variation1nstd206human GRCh38 chr8: 69,999,352-70,051,284 , GRCh37.p13 chr8: 70,911,587-70,963,519 PRDM14
    nsv5479878copy number variation1nstd206human GRCh38 chr8: 70,064,745-70,065,106 , GRCh37.p13 chr8: 70,976,980-70,977,341 PRDM14
    nsv5330192translocation1nstd200human GRCh37 chr8: 70,962,651-70,962,651 , GRCh37 chr8: 70,954,357-70,954,357 , GRCh38.p12 chr8: 70,042,122-70,042,122 , GRCh38.p12 chr8: 70,050,416-70,050,416 PRDM14
    nsv5311834copy number variation1nstd204human GRCh38.p13 chr8: 69,999,346-70,051,288 , GRCh37.p13 chr8: 70,911,581-70,963,523 PRDM14
    nsv4965446copy number variation1nstd200human GRCh38 chr8: 70,063,546-70,084,253 , GRCh37.p13 chr8: 70,975,781-70,996,488 RNU1-101P, PRDM14
    nsv4965445copy number variation1nstd200human GRCh38 chr8: 70,056,764-70,062,759 , GRCh37.p13 chr8: 70,968,999-70,974,994 PRDM14
    nsv4965444copy number variation1nstd200human GRCh38 chr8: 69,999,352-70,051,284 , GRCh37.p13 chr8: 70,911,587-70,963,519 PRDM14
    nsv4829077copy number variation1nstd200human GRCh37 chr8: 70,975,781-70,996,488 , GRCh38.p12 chr8: 70,063,546-70,084,253 RNU1-101P, PRDM14
    nsv4829076copy number variation1nstd200human GRCh37 chr8: 70,911,587-70,963,519 , GRCh38.p12 chr8: 69,999,352-70,051,284 PRDM14
    nsv4829075copy number variation1nstd200human GRCh37 chr8: 70,880,653-71,012,109 , GRCh38.p12 chr8: 69,968,418-70,099,874 RNU1-101P, SUMO2P20, 1 more genes
    nsv4737417copy number variation1nstd199human GRCh37 chr8: 70,975,466-70,975,585 , GRCh38.p12 chr8: 70,063,231-70,063,350 PRDM14
    nsv4675545copy number variation1nstd102humanUncertain significance GRCh37 chr8: 70,848,713-71,632,067 , GRCh38.p12 chr8: 69,936,478-70,719,832 SDCBPP2, RNY3P14, 16 more genes
    nsv4599690copy number variation1nstd183human GRCh37 chr8: 70,890,665-70,994,109 , GRCh38.p12 chr8: 69,978,430-70,081,874 PRDM14, RNU1-101P, 1 more genes
    nsv4496343mobile element insertion1nstd166human GRCh37.p13 chr8: 70,974,490-70,974,490 , GRCh38.p12 chr8: 70,062,255-70,062,255 PRDM14
    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
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
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