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Items: 1 to 20 of 456

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7065305inversion1nstd229human GRCh38 chr8: 22,279,743-22,573,171 , GRCh37.p13 chr8: 22,137,256-22,430,684 SLC39A14, RPL21P77, 5 more genes
    nsv6853352copy number variation1nstd229human GRCh38 chr8: 22,293,401-22,364,700 , GRCh37.p13 chr8: 22,150,914-22,222,213 PIWIL2
    nsv6852898copy number variation1nstd229human GRCh38 chr8: 22,279,801-22,564,100 , GRCh37.p13 chr8: 22,137,314-22,421,613 PPP3CC, PIWIL2, 5 more genes
    nsv6850367copy number variation1nstd229human GRCh38 chr8: 22,353,101-22,396,600 , GRCh37.p13 chr8: 22,210,614-22,254,113 PIWIL2, RPL21P77, 1 more genes
    nsv6850189copy number variation1nstd229human GRCh38 chr8: 22,282,636-22,521,757 , GRCh37.p13 chr8: 22,140,149-22,379,270 PPP3CC, PIWIL2, 4 more genes
    nsv6849815copy number variation1nstd229human GRCh38 chr8: 22,331,151-22,334,404 , GRCh37.p13 chr8: 22,188,664-22,191,917 PIWIL2
    nsv6848523copy number variation1nstd229human GRCh38 chr8: 22,301,437-22,305,337 , GRCh37.p13 chr8: 22,158,950-22,162,850 PIWIL2
    nsv6846723copy number variation1nstd229human GRCh38 chr8: 22,341,498-22,350,500 , GRCh37.p13 chr8: 22,199,011-22,208,013 PIWIL2
    nsv6845542copy number variation1nstd229human GRCh38 chr8: 22,323,392-22,325,758 , GRCh37.p13 chr8: 22,180,905-22,183,271 PIWIL2
    nsv6842532copy number variation1nstd229human GRCh38 chr8: 21,982,501-22,396,600 , GRCh37.p13 chr8: 21,840,012-22,254,113 SFTPC, BMP1, 16 more genes
    nsv6842345copy number variation1nstd229human GRCh38 chr8: 21,739,201-22,308,765 , GRCh37.p13 chr8: 21,596,713-22,166,278 FHIP2B, FGF17, 17 more genes
    nsv6841437copy number variation1nstd229human GRCh38 chr8: 22,345,274-22,345,301 , GRCh37.p13 chr8: 22,202,787-22,202,814 PIWIL2
    nsv6840248copy number variation1nstd229human GRCh38 chr8: 22,345,401-22,348,100 , GRCh37.p13 chr8: 22,202,914-22,205,613 PIWIL2
    nsv6839801copy number variation1nstd229human GRCh38 chr8: 22,281,683-22,281,719 , GRCh37.p13 chr8: 22,139,196-22,139,232 PIWIL2
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6572948inversion1nstd223human GRCh38 chr8: 22,350,352-22,351,692 , GRCh37.p13 chr8: 22,207,865-22,209,205 PIWIL2
    nsv6569109inversion1nstd223human GRCh38 chr8: 22,293,550-22,294,359 , GRCh37.p13 chr8: 22,151,063-22,151,872 PIWIL2
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