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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5895376copy number variation1nstd209human GRCh38 chr3: 133,603,659-133,605,404 , GRCh37.p13 chr3: 133,322,503-133,324,248 TOPBP1
    nsv5834609copy number variation1nstd209human GRCh38 chr3: 133,603,636-133,605,415 , GRCh37.p13 chr3: 133,322,480-133,324,259 TOPBP1
    nsv5572107copy number variation1nstd207human GRCh38 chr3: 133,603,659-133,605,404 , GRCh37.p13 chr3: 133,322,503-133,324,248 TOPBP1
    nsv5452407copy number variation1nstd206human GRCh38 chr3: 133,603,661-133,605,405 , GRCh37.p13 chr3: 133,322,505-133,324,249 TOPBP1
    nsv5388061copy number variation1nstd186human GRCh37 chr3: 133,322,505-133,324,249 , GRCh38.p12 chr3: 133,603,661-133,605,405 TOPBP1
    nsv5351970translocation1nstd200human GRCh38 chr3: 133,623,310-133,623,310 , GRCh38 chr3: 133,623,195-133,623,195 , GRCh37.p13 chr3: 133,342,154-133,342,154 , GRCh37.p13 chr3: 133,342,039-133,342,039 TOPBP1
    nsv5351969translocation1nstd200human GRCh38 chr3: 133,623,090-133,623,090 , GRCh38 chr3: 133,620,349-133,620,349 , GRCh37.p13 chr3: 133,339,193-133,339,193 , GRCh37.p13 chr3: 133,341,934-133,341,934 TOPBP1
    nsv5351968translocation1nstd200human GRCh38 chr3: 133,618,435-133,618,435 , GRCh38 chr3: 133,620,153-133,620,153 , GRCh37.p13 chr3: 133,338,997-133,338,997 , GRCh37.p13 chr3: 133,337,279-133,337,279 TOPBP1
    nsv5351967translocation1nstd200human GRCh38 chr3: 133,617,327-133,617,327 , GRCh38 chr3: 133,618,212-133,618,212 , GRCh37.p13 chr3: 133,337,056-133,337,056 , GRCh37.p13 chr3: 133,336,171-133,336,171 TOPBP1
    nsv5351966translocation1nstd200human GRCh38 chr3: 133,616,811-133,616,811 , GRCh38 chr3: 133,612,554-133,612,554 , GRCh37.p13 chr3: 133,331,398-133,331,398 , GRCh37.p13 chr3: 133,335,655-133,335,655 TOPBP1
    nsv5351965translocation1nstd200human GRCh38 chr3: 133,608,964-133,608,964 , GRCh38 chr3: 133,611,002-133,611,002 , GRCh37.p13 chr3: 133,327,808-133,327,808 , GRCh37.p13 chr3: 133,329,846-133,329,846 TOPBP1
    nsv5351963translocation1nstd200human GRCh38 chr3: 133,608,870-133,608,870 , GRCh38 chr3: 133,608,698-133,608,698 , GRCh37.p13 chr3: 133,327,714-133,327,714 , GRCh37.p13 chr3: 133,327,542-133,327,542 TOPBP1
    nsv5345443translocation1nstd200human GRCh37 chr3: 133,339,193-133,339,193 , GRCh37 chr3: 133,341,934-133,341,934 , GRCh38.p12 chr3: 133,620,349-133,620,349 , GRCh38.p12 chr3: 133,623,090-133,623,090 TOPBP1
    nsv5342402translocation1nstd200human GRCh37 chr3: 133,331,398-133,331,398 , GRCh37 chr3: 133,335,655-133,335,655 , GRCh38.p12 chr3: 133,612,554-133,612,554 , GRCh38.p12 chr3: 133,616,811-133,616,811 TOPBP1
    nsv5339611translocation1nstd200human GRCh37 chr3: 133,338,997-133,338,997 , GRCh37 chr3: 133,337,279-133,337,279 , GRCh38.p12 chr3: 133,618,435-133,618,435 , GRCh38.p12 chr3: 133,620,153-133,620,153 TOPBP1
    nsv5339364translocation1nstd200human GRCh37 chr3: 133,329,846-133,329,846 , GRCh37 chr3: 133,327,808-133,327,808 , GRCh38.p12 chr3: 133,611,002-133,611,002 , GRCh38.p12 chr3: 133,608,964-133,608,964 TOPBP1
    nsv5338395translocation1nstd200human GRCh37 chr3: 133,342,301-133,342,301 , GRCh37 chr3: 133,342,895-133,342,895 , GRCh38.p12 chr3: 133,624,051-133,624,051 , GRCh38.p12 chr3: 133,623,457-133,623,457 TOPBP1
    nsv5331431translocation1nstd200human GRCh37 chr3: 133,327,714-133,327,714 , GRCh37 chr3: 133,327,542-133,327,542 , GRCh38.p12 chr3: 133,608,870-133,608,870 , GRCh38.p12 chr3: 133,608,698-133,608,698 TOPBP1
    nsv5330464translocation1nstd200human GRCh37 chr3: 133,337,056-133,337,056 , GRCh37 chr3: 133,336,171-133,336,171 , GRCh38.p12 chr3: 133,617,327-133,617,327 , GRCh38.p12 chr3: 133,618,212-133,618,212 TOPBP1
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