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Items: 1 to 20 of 658

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141333copy number variation1nstd232human GRCh37.p13 chr6: 10,589,539-10,589,596 , GRCh38.p12 chr6: 10,589,306-10,589,363 , GRCh38.p12 chr6|NW_018654713.1: 100,190-100,247 GCNT2
    nsv7097170copy number variation1nstd102humanPathogenic GRCh37 chr6: 10,556,657-10,626,840 , GRCh38.p12 chr6|NW_018654713.1: 67,308-137,491 , GRCh38.p12 chr6: 10,556,424-10,626,607 RPL21P63, GCNT2
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7042773inversion1nstd229human GRCh38 chr6: 8,542,608-11,835,677 , GRCh37.p13 chr6: 8,542,841-11,835,910 LOC112267952, RNU1-64P, 51 more genes
    nsv6798080copy number variation1nstd229human GRCh38 chr6: 10,465,601-10,536,400 , GRCh37.p13 chr6: 10,465,834-10,536,633 LOC100422564, LOC101928146, 2 more genes
    nsv6797878copy number variation1nstd229human GRCh38 chr6: 10,616,183-10,616,285 , GRCh37.p13 chr6: 10,616,416-10,616,518 GCNT2
    nsv6797191copy number variation1nstd229human GRCh38 chr6: 10,589,607-10,593,617 , GRCh37.p13 chr6: 10,589,840-10,593,850 GCNT2
    nsv6797190copy number variation1nstd229human GRCh38 chr6: 10,589,601-10,593,600 , GRCh37.p13 chr6: 10,589,834-10,593,833 GCNT2
    nsv6796694copy number variation1nstd229human GRCh38 chr6: 10,600,901-10,604,100 , GRCh37.p13 chr6: 10,601,134-10,604,333 GCNT2
    nsv6795539copy number variation1nstd229human GRCh38 chr6: 10,534,937-10,563,044 , GRCh37.p13 chr6: 10,535,170-10,563,277 GCNT2
    nsv6794854copy number variation1nstd229human GRCh38 chr6: 10,589,306-10,589,364 , GRCh37.p13 chr6: 10,589,539-10,589,597 GCNT2
    nsv6794057copy number variation1nstd229human GRCh38 chr6: 10,467,817-10,530,962 , GRCh37.p13 chr6: 10,468,050-10,531,195 LOC100422564, LOC101928146, 2 more genes
    nsv6793316copy number variation1nstd229human GRCh38 chr6: 10,520,792-10,522,311 , GRCh37.p13 chr6: 10,521,025-10,522,544 GCNT2, LOC101928146
    nsv6791608copy number variation1nstd229human GRCh38 chr6: 10,503,561-10,553,640 , GRCh37.p13 chr6: 10,503,794-10,553,873 GCNT2, LOC101928146, 1 more genes
    nsv6789192copy number variation1nstd229human GRCh38 chr6: 10,495,714-10,615,494 , GRCh37.p13 chr6: 10,495,947-10,615,727 GCNT2, LOC100422564, 2 more genes
    nsv6788833copy number variation1nstd229human GRCh38 chr6: 10,591,102-10,600,623 , GRCh37.p13 chr6: 10,591,335-10,600,856 GCNT2
    nsv6786418copy number variation1nstd229human GRCh38 chr6: 10,610,701-10,617,900 , GRCh37.p13 chr6: 10,610,934-10,618,133 GCNT2
    nsv6785283copy number variation1nstd229human GRCh38 chr6: 10,538,549-10,543,443 , GRCh37.p13 chr6: 10,538,782-10,543,676 GCNT2
    nsv6784837copy number variation1nstd229human GRCh38 chr6: 10,530,688-10,604,648 , GRCh37.p13 chr6: 10,530,921-10,604,881 GCNT2, RPL21P63
    nsv6783900copy number variation1nstd229human GRCh38 chr6: 10,611,160-10,611,247 , GRCh37.p13 chr6: 10,611,393-10,611,480 GCNT2
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