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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
    nsv5917237copy number variation1nstd209human GRCh38 chr8: 28,318,306-28,318,356 , GRCh37.p13 chr8: 28,175,823-28,175,873 PNOC
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5118122mobile element insertion1nstd203human GRCh38 chr8: 28,330,578-28,330,625 , GRCh37.p13 chr8: 28,188,095-28,188,142 PNOC
    nsv5112179mobile element insertion1nstd203human GRCh38 chr8: 28,330,362-28,330,412 , GRCh37.p13 chr8: 28,187,879-28,187,929 PNOC
    nsv5112038mobile element insertion1nstd203human GRCh38 chr8: 28,330,560-28,330,578 , GRCh37.p13 chr8: 28,188,077-28,188,095 PNOC
    nsv4959878copy number variation1nstd200human GRCh38 chr8: 28,336,035-28,336,165 , GRCh37.p13 chr8: 28,193,552-28,193,682 PNOC
    nsv4959877copy number variation1nstd200human GRCh38 chr8: 28,321,533-28,328,866 , GRCh37.p13 chr8: 28,179,050-28,186,383 PNOC
    nsv4821620copy number variation1nstd200human GRCh37 chr8: 28,193,552-28,193,682 , GRCh38.p12 chr8: 28,336,035-28,336,165 PNOC
    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
    nsv4733137copy number variation1nstd199human GRCh37 chr8: 28,185,312-28,185,872 , GRCh38.p12 chr8: 28,327,795-28,328,355 PNOC
    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
    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
    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
    nsv3924532copy number variation1nstd102humanPathogenic NCBI36 chr8: 181,605-31,068,132 , GRCh38 chr8: 241,605-31,091,074 , GRCh37 chr8: 191,605-30,948,590 DEFB109B, GATA4, 585 more genes
    nsv3923600copy number variation1nstd102humanPathogenic NCBI36 chr8: 12,284,724-28,539,000 , GRCh37 chr8: 12,240,353-28,483,081 , GRCh38 chr8: 12,382,844-28,625,564 LOC105379340, LOC646708, 259 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 BNIP3L, RNU6-178P, 123 more genes
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