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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941221copy number variation1nstd209human GRCh38 chr20: 524,303-524,609 , GRCh37.p13 chr20: 504,947-505,253 CSNK2A1
    nsv5939427copy number variation1nstd209human GRCh38 chr20: 505,558-506,071 , GRCh37.p13 chr20: 486,202-486,715 CSNK2A1
    nsv5936542copy number variation1nstd209human GRCh38 chr20: 524,708-525,650 , GRCh37.p13 chr20: 505,352-506,294 CSNK2A1
    nsv5931598copy number variation1nstd209human GRCh38 chr20: 475,971-476,188 , GRCh37.p13 chr20: 456,615-456,832 CSNK2A1
    nsv5867774copy number variation1nstd209human GRCh38 chr20: 506,570-508,269 , GRCh37.p13 chr20: 487,214-488,913 CSNK2A1
    nsv5727563mobile element insertion1nstd211human GRCh38 chr20: 521,240-521,240 , GRCh37.p13 chr20: 501,884-501,884 CSNK2A1
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5531441copy number variation1nstd206human GRCh38 chr20: 505,570-506,045 , GRCh37.p13 chr20: 486,214-486,689 CSNK2A1
    nsv5524491copy number variation1nstd206human GRCh38 chr20: 397,311-501,964 , GRCh37.p13 chr20: 377,955-482,608 CSNK2A1, TBC1D20, 2 more genes
    nsv5521240copy number variation1nstd206human GRCh38 chr20: 476,996-477,101 , GRCh37.p13 chr20: 457,640-457,745 CSNK2A1
    nsv5520299copy number variation1nstd206human GRCh38 chr20: 523,742-525,643 , GRCh37.p13 chr20: 504,386-506,287 CSNK2A1
    nsv5516652copy number variation1nstd206human GRCh38 chr20: 505,535-506,072 , GRCh37.p13 chr20: 486,179-486,716 CSNK2A1
    nsv5516212copy number variation1nstd206human GRCh38 chr20: 500,836-501,226 , GRCh37.p13 chr20: 481,480-481,870 CSNK2A1
    nsv5381806copy number variation1nstd102humanPathogenic GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198 DEFB132, LOC101929937, 24 more genes
    nsv5359984translocation1nstd200human GRCh38 chr20: 526,200-526,200 , GRCh38 chr20: 525,731-525,731 , GRCh37.p13 chr20: 506,844-506,844 , GRCh37.p13 chr20: 506,375-506,375 CSNK2A1
    nsv5323494copy number variation1nstd204human GRCh38.p13 chr20: 500,825-501,187 , GRCh37.p13 chr20: 481,469-481,831 CSNK2A1
    nsv5292945copy number variation1nstd204human GRCh38.p13 chr20: 523,413-525,512 , GRCh37.p13 chr20: 504,057-506,156 CSNK2A1
    nsv5028309copy number variation1nstd200human GRCh38 chr20: 524,193-525,710 , GRCh37.p13 chr20: 504,837-506,354 CSNK2A1
    nsv5028308copy number variation1nstd200human GRCh38 chr20: 475,971-476,189 , GRCh37.p13 chr20: 456,615-456,833 CSNK2A1
    nsv5025043copy number variation1nstd200human GRCh38 chr20: 543,127-572,323 , GRCh37.p13 chr20: 523,771-552,967 CSNK2A1
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