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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955305insertion1nstd209human GRCh38 chr8: 41,299,577-41,299,577 , GRCh37.p13 chr8: 41,157,096-41,157,096 SFRP1
    nsv5919670copy number variation1nstd209human GRCh38 chr8: 41,280,473-41,280,821 , GRCh37.p13 chr8: 41,137,992-41,138,340 SFRP1
    nsv5918657copy number variation1nstd209human GRCh38 chr8: 41,267,321-41,269,835 , GRCh37.p13 chr8: 41,124,840-41,127,354 SFRP1, RPS29P2, 1 more genes
    nsv5917461copy number variation1nstd209human GRCh38 chr8: 41,299,580-47,196,853 , GRCh37.p13 chr8: 41,157,099-48,108,476 , AFG3L2P1, 81 more genes
    nsv5865014copy number variation1nstd209human GRCh38 chr8: 41,267,339-41,269,898 , GRCh37.p13 chr8: 41,124,858-41,127,417 SFRP1, RPS29P2, 1 more genes
    nsv5632112insertion1nstd207human GRCh38 chr8: 41,299,577-41,299,577 , GRCh37.p13 chr8: 41,157,096-41,157,096 SFRP1
    nsv5541476insertion1nstd206human GRCh38 chr8: 41,299,577-41,299,577 , GRCh37.p13 chr8: 41,157,096-41,157,096 SFRP1
    nsv5482993copy number variation1nstd206human GRCh38 chr8: 41,287,952-41,288,589 , GRCh37.p13 chr8: 41,145,471-41,146,108 SFRP1
    nsv5477719copy number variation1nstd206human GRCh38 chr8: 41,270,349-41,271,002 , GRCh37.p13 chr8: 41,127,868-41,128,521 MIR548AO, SFRP1, 1 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5118801mobile element insertion1nstd203human GRCh38 chr8: 41,299,569-41,299,577 , GRCh37.p13 chr8: 41,157,088-41,157,096 SFRP1
    nsv5117734mobile element insertion1nstd203human GRCh38 chr8: 41,299,578-41,299,582 , GRCh37.p13 chr8: 41,157,097-41,157,101 SFRP1
    nsv5114838mobile element insertion1nstd203human GRCh38 chr8: 41,299,664-41,299,664 , GRCh37.p13 chr8: 41,157,183-41,157,183 SFRP1
    nsv5113794mobile element insertion1nstd203human GRCh38 chr8: 41,299,579-41,299,584 , GRCh37.p13 chr8: 41,157,098-41,157,103 SFRP1
    nsv5112769mobile element insertion1nstd203human GRCh38 chr8: 41,299,577-41,299,577 , GRCh37.p13 chr8: 41,157,096-41,157,096 SFRP1
    nsv5111184mobile element insertion1nstd203human GRCh38 chr8: 41,290,886-41,290,924 , GRCh37.p13 chr8: 41,148,405-41,148,443 SFRP1
    nsv5108987mobile element insertion1nstd203human GRCh38 chr8: 41,299,584-41,299,584 , GRCh37.p13 chr8: 41,157,103-41,157,103 SFRP1
    nsv5106825mobile element insertion1nstd203human GRCh38 chr8: 41,299,576-41,299,580 , GRCh37.p13 chr8: 41,157,095-41,157,099 SFRP1
    nsv5101446mobile element insertion1nstd203human GRCh38 chr8: 41,299,580-41,299,584 , GRCh37.p13 chr8: 41,157,099-41,157,103 SFRP1
    nsv4960374copy number variation1nstd200human GRCh38 chr8: 41,280,796-41,283,592 , GRCh37.p13 chr8: 41,138,315-41,141,111 SFRP1
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