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Items: 1 to 20 of 251

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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
    nsv6856612copy number variation1nstd229human GRCh38 chr8: 22,991,008-22,991,168 , GRCh37.p13 chr8: 22,848,521-22,848,681 RHOBTB2, LOC107984124
    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
    nsv6854056copy number variation1nstd229human GRCh38 chr8: 22,970,778-22,993,888 , GRCh37.p13 chr8: 22,828,291-22,851,401 RN7SL303P, RHOBTB2, 1 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
    nsv6850468copy number variation1nstd229human GRCh38 chr8: 22,985,852-22,992,939 , GRCh37.p13 chr8: 22,843,365-22,850,452 LOC107984124, RHOBTB2
    nsv6846849copy number variation1nstd229human GRCh38 chr8: 23,013,017-23,013,536 , GRCh37.p13 chr8: 22,870,530-22,871,049 RHOBTB2
    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
    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
    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
    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
    nsv6428588copy number variation1nstd223human GRCh38 chr8: 23,012,965-23,013,657 , GRCh37.p13 chr8: 22,870,478-22,871,170 RHOBTB2
    nsv6427391copy number variation1nstd223human GRCh38 chr8: 22,998,618-23,011,146 , GRCh37.p13 chr8: 22,856,131-22,868,659 LOC107984124, RHOBTB2
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
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