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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961369insertion1nstd209human GRCh38 chr5: 141,407,491-141,407,491 , GRCh37.p13 chr5: 140,787,058-140,787,058 PCDHGB6, PCDHGB2, 14 more genes
    nsv5896403copy number variation1nstd209human GRCh38 chr5: 141,393,101-141,403,239 , GRCh37.p13 chr5: 140,772,668-140,782,806 PCDHGA2, PCDHGA4, 13 more genes
    nsv5892008copy number variation1nstd209human GRCh38 chr5: 141,480,504-141,482,778 , GRCh37.p13 chr5: 140,860,071-140,862,345 PCDHGC3, PCDHGA2, 19 more genes
    nsv5841789copy number variation1nstd209human GRCh38 chr5: 141,407,682-141,417,857 , GRCh37.p13 chr5: 140,787,249-140,797,424 PCDHGA6, PCDHGB2, 16 more genes
    nsv5841161copy number variation1nstd209human GRCh38 chr5: 141,480,497-141,482,796 , GRCh37.p13 chr5: 140,860,064-140,862,363 PCDHGB5, PCDHGA7, 19 more genes
    nsv5676892mobile element insertion2nstd211human GRCh38 chr5: 141,407,505-141,407,505 , GRCh37.p13 chr5: 140,787,072-140,787,072 PCDHG@, PCDHGA3, 14 more genes
    nsv5638498insertion1nstd207human GRCh38 chr5: 141,407,491-141,407,491 , GRCh37.p13 chr5: 140,787,058-140,787,058 PCDHGA4, PCDHGA1, 14 more genes
    nsv5638473insertion1nstd207human GRCh38 chr5: 141,508,683-141,508,683 , GRCh37.p13 chr5: 140,888,250-140,888,250 PCDHGA6, PCDHGA10, 21 more genes
    nsv5628287insertion1nstd207human GRCh38 chr5: 141,482,759-141,482,759 , GRCh37.p13 chr5: 140,862,326-140,862,326 PCDHGB5, PCDHGA1, 19 more genes
    nsv5554312sequence alteration1nstd206human GRCh38 chr5: 141,482,755-141,482,779 , GRCh37.p13 chr5: 140,862,322-140,862,346 PCDHGB1, PCDHGA9, 19 more genes
    nsv5547503insertion1nstd206human GRCh38 chr5: 141,482,755-141,482,755 , GRCh37.p13 chr5: 140,862,322-140,862,322 PCDHGA7, PCDHGA11, 19 more genes
    nsv5473096copy number variation1nstd206human GRCh38 chr5: 141,407,659-141,418,000 , GRCh37.p13 chr5: 140,787,226-140,797,567 PCDHGA8, PCDHGA10, 16 more genes
    nsv5467763copy number variation1nstd206human GRCh38 chr5: 141,407,885-141,418,104 , GRCh37.p13 chr5: 140,787,452-140,797,671 PCDHGB2, PCDHGB6, 16 more genes
    nsv5461362copy number variation1nstd206human GRCh38 chr5: 141,463,888-141,464,854 , GRCh37.p13 chr5: 140,843,455-140,844,421 PCDHGB6, PCDHGB2, 18 more genes
    nsv5459155copy number variation1nstd206human GRCh38 chr5: 141,414,792-141,432,795 , GRCh37.p13 chr5: 140,794,359-140,812,362 PCDHG@, PCDHGA12, 19 more genes
    nsv5406687mobile element insertion1nstd206human GRCh38 chr5: 141,407,505-141,407,556 , GRCh37.p13 chr5: 140,787,072-140,787,123 PCDHGA8, PCDHGB4, 14 more genes
    nsv5381510copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,633,338-140,998,481 , GRCh38.p12 chr5: 137,297,649-141,618,914 RNA5SP195, LOC112267855, 174 more genes
    nsv5378123translocation1nstd200human GRCh38 chr5: 141,480,504-141,480,504 , GRCh38 chr5: 141,482,779-141,482,779 , GRCh37.p13 chr5: 140,862,346-140,862,346 , GRCh37.p13 chr5: 140,860,071-140,860,071 PCDHGB4, PCDHGB3, 19 more genes
    nsv5340192translocation1nstd200human GRCh37 chr5: 140,860,071-140,860,071 , GRCh37 chr5: 140,862,346-140,862,346 , GRCh38.p12 chr5: 141,482,779-141,482,779 , GRCh38.p12 chr5: 141,480,504-141,480,504 PCDHGA1, PCDHGA8, 19 more genes
    nsv5320741translocation1nstd204human GRCh37.p13 chr5: 140,860,071-140,860,071 , GRCh37.p13 chr5: 140,862,346-140,862,346 , GRCh38.p13 chr5: 141,482,779-141,482,779 , GRCh38.p13 chr5: 141,480,504-141,480,504 PCDHGB4, PCDHGB3, 19 more genes
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