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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5488826copy number variation1nstd206human GRCh38 chr8: 28,381,309-28,388,537 , GRCh37.p13 chr8: 28,238,826-28,246,054 ZNF395
    nsv5486690copy number variation1nstd206human GRCh38 chr8: 28,351,218-28,351,328 , GRCh37.p13 chr8: 28,208,735-28,208,845 ZNF395
    nsv5300525copy number variation1nstd204human GRCh38.p13 chr8: 28,386,620-28,386,747 , GRCh37.p13 chr8: 28,244,137-28,244,264 ZNF395
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5114473mobile element insertion1nstd203human GRCh38 chr8: 28,376,318-28,376,327 , GRCh37.p13 chr8: 28,233,835-28,233,844 ZNF395
    nsv4959880copy number variation1nstd200human GRCh38 chr8: 28,386,629-28,386,739 , GRCh37.p13 chr8: 28,244,146-28,244,256 ZNF395
    nsv4959879copy number variation1nstd200human GRCh38 chr8: 28,365,638-28,365,715 , GRCh37.p13 chr8: 28,223,155-28,223,232 ZNF395
    nsv4954289copy number variation1nstd200human GRCh38 chr8: 28,376,751-28,543,567 , GRCh37.p13 chr8: 28,234,268-28,401,084 FZD3, MIR4288, 4 more genes
    nsv4954288copy number variation1nstd200human GRCh38 chr8: 28,368,853-28,376,265 , GRCh37.p13 chr8: 28,226,370-28,233,782 ZNF395
    nsv4821621copy number variation1nstd200human GRCh37 chr8: 28,233,091-28,234,173 , GRCh38.p12 chr8: 28,375,574-28,376,656 ZNF395
    nsv4768211inversion1nstd199human GRCh37 chr8: 23,474,464-53,327,098 , GRCh38.p12 chr8: 23,616,951-52,414,538 , ADRA1A, 411 more genes
    nsv4756879inversion1nstd199human GRCh37 chr8: 23,474,453-53,323,933 , GRCh38.p12 chr8: 23,616,940-52,411,373 , ADRA1A, 411 more genes
    nsv4728911copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,528,482-29,886,483 , GRCh38.p12 chr8: 12,670,973-30,028,967 NAT1, NAT2, 272 more genes
    nsv4675292copy number variation1nstd102humanPathogenic GRCh37 chr8: 24,305,969-28,673,405 , GRCh38.p12 chr8: 24,448,456-28,815,888 LOC112268023, GNRH1, 79 more genes
    nsv4615773copy number variation1nstd183human GRCh37 chr8: 28,238,804-28,246,288 , GRCh38.p12 chr8: 28,381,287-28,388,771 ZNF395
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4348018copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,546,855-35,816,855 , GRCh38.p12 chr8: 12,689,346-35,959,337 NAT1, NAT2, 343 more genes
    nsv4157022copy number variation1nstd166human GRCh37.p13 chr8: 28,203,725-28,203,833 , GRCh38.p12 chr8: 28,346,208-28,346,316 ZNF395
    nsv4154353copy number variation1nstd166human GRCh37.p13 chr8: 28,207,435-28,207,496 , GRCh38.p12 chr8: 28,349,918-28,349,979 ZNF395
    nsv3972390copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 12,556,004-34,374,150 , GRCh38.p12 chr8: 12,698,495-34,516,632 NAT1, NAT2, 335 more genes
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