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Items: 1 to 20 of 227

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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
    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
    nsv6851806copy number variation1nstd229human GRCh38 chr8: 23,073,988-23,076,938 , GRCh37.p13 chr8: 22,931,501-22,934,451 LOC286059
    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
    nsv6843351copy number variation1nstd229human GRCh38 chr8: 23,078,454-23,079,734 , GRCh37.p13 chr8: 22,935,967-22,937,247 LOC286059
    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
    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
    nsv6572780inversion1nstd223human GRCh38 chr8: 23,076,670-23,077,394 , GRCh37.p13 chr8: 22,934,183-22,934,907 LOC286059
    nsv6565031inversion1nstd223human GRCh38 chr8: 22,900,235-30,247,902 , GRCh37.p13 chr8: 22,757,748-30,105,418 LOC105379349, MIR6876, 140 more genes
    nsv6429716copy number variation1nstd223human GRCh38 chr8: 22,969,514-24,288,515 , GRCh37.p13 chr8: 22,827,027-24,146,028 NKX3-1, LOC107984124, 27 more genes
    nsv6417198copy number variation1nstd223human GRCh38 chr8: 23,029,981-23,202,291 , GRCh37.p13 chr8: 22,887,494-23,059,804 TNFRSF10B, LOC254896, 4 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
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