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Items: 1 to 20 of 359

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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
    nsv7146582insertion1nstd232human GRCh37.p13 chr8: 22,886,116-22,886,116 , GRCh38.p12 chr8: 23,028,603-23,028,603 TNFRSF10B
    nsv7140439copy number variation1nstd232human GRCh37.p13 chr8: 22,897,787-22,897,838 , GRCh38.p12 chr8: 23,040,274-23,040,325 TNFRSF10B
    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
    nsv7074761inversion1nstd229human GRCh38 chr8: 22,699,805-23,128,957 , GRCh37.p13 chr8: 22,557,318-22,986,470 LOC105379325, LOC101929237, 10 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv6856450copy number variation1nstd229human GRCh38 chr8: 22,919,504-23,266,199 , GRCh37.p13 chr8: 22,777,017-23,123,712 CHMP7, LOC254896, 11 more genes
    nsv6852401copy number variation1nstd229human GRCh38 chr8: 22,941,093-23,155,466 , GRCh37.p13 chr8: 22,798,606-23,012,979 TNFRSF10C, RHOBTB2, 7 more genes
    nsv6847684copy number variation1nstd229human GRCh38 chr8: 23,057,026-23,057,438 , GRCh37.p13 chr8: 22,914,539-22,914,951 TNFRSF10B
    nsv6844842copy number variation1nstd229human GRCh38 chr8: 23,056,401-23,332,600 , GRCh37.p13 chr8: 22,913,914-23,190,113 TNFRSF10B, LOC286059, 9 more genes
    nsv6842954copy number variation1nstd229human GRCh38 chr8: 22,958,501-23,751,500 , GRCh37.p13 chr8: 22,816,014-23,609,013 TNFRSF10B, RNU4-71P, 23 more genes
    nsv6840977copy number variation1nstd229human GRCh38 chr8: 23,048,964-23,056,752 , GRCh37.p13 chr8: 22,906,477-22,914,265 TNFRSF10B
    nsv6840067copy number variation1nstd229human GRCh38 chr8: 22,757,016-23,054,950 , GRCh37.p13 chr8: 22,614,529-22,912,463 RN7SL303P, PEBP4, 6 more genes
    nsv6839384copy number variation1nstd229human GRCh38 chr8: 23,047,233-23,048,312 , GRCh37.p13 chr8: 22,904,746-22,905,825 TNFRSF10B
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632540copy number variation1nstd224human GRCh37 chr8: 22,844,981-23,104,413 , GRCh38.p12 chr8: 22,987,468-23,246,900 TNFRSF10C, TNFRSF10A, 9 more genes
    nsv6575483inversion1nstd223human GRCh38 chr8: 23,066,788-23,067,122 , GRCh37.p13 chr8: 22,924,301-22,924,635 LOC286059, TNFRSF10B
    nsv6573637inversion1nstd223human GRCh38 chr8: 23,058,059-23,058,606 , GRCh37.p13 chr8: 22,915,572-22,916,119 TNFRSF10B
    nsv6573131inversion1nstd223human GRCh38 chr8: 23,056,664-23,057,083 , GRCh37.p13 chr8: 22,914,177-22,914,596 TNFRSF10B
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