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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891543copy number variation1nstd209human GRCh38 chr6: 155,305,199-155,305,637 , GRCh37.p13 chr6: 155,626,333-155,626,771 TFB1M
    nsv5679893mobile element insertion1nstd211human GRCh38 chr6: 155,296,451-155,296,451 , GRCh37.p13 chr6: 155,617,585-155,617,585 TFB1M
    nsv5639249insertion1nstd207human GRCh38 chr6: 155,305,480-155,305,480 , GRCh37.p13 chr6: 155,626,614-155,626,614 TFB1M
    nsv5639007insertion1nstd207human GRCh38 chr6: 155,234,961-155,234,961 , GRCh37.p13 chr6: 155,556,095-155,556,095 TFB1M, TIAM2
    nsv5580686copy number variation1nstd207human GRCh38 chr6: 155,286,489-155,286,540 , GRCh37.p13 chr6: 155,607,623-155,607,674 TFB1M
    nsv5576708copy number variation1nstd207human GRCh38 chr6: 155,305,331-155,305,547 , GRCh37.p13 chr6: 155,626,465-155,626,681 TFB1M
    nsv5570345copy number variation1nstd207human GRCh38 chr6: 155,305,196-155,305,271 , GRCh37.p13 chr6: 155,626,330-155,626,405 TFB1M
    nsv5567439copy number variation1nstd207human GRCh38 chr6: 155,305,488-155,305,559 , GRCh37.p13 chr6: 155,626,622-155,626,693 TFB1M
    nsv5462094copy number variation1nstd206human GRCh38 chr6: 155,290,418-155,290,541 , GRCh37.p13 chr6: 155,611,552-155,611,675 TFB1M
    nsv5456927copy number variation1nstd206human GRCh38 chr6: 155,263,574-155,273,297 , GRCh37.p13 chr6: 155,584,708-155,594,431 CLDN20, TFB1M
    nsv5381779copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,308,263-158,394,005 , GRCh38.p12 chr6: 154,987,129-157,972,973 TFB1M, ARID1B, 30 more genes
    nsv5369956translocation1nstd200human GRCh38 chr6: 155,305,862-155,305,862 , GRCh38 chr6: 155,305,150-155,305,150 , GRCh37.p13 chr6: 155,626,284-155,626,284 , GRCh37.p13 chr6: 155,626,996-155,626,996 TFB1M
    nsv4943549copy number variation1nstd200human GRCh38 chr6: 155,279,284-155,282,742 , GRCh37.p13 chr6: 155,600,418-155,603,876 TFB1M
    nsv4943548copy number variation1nstd200human GRCh38 chr6: 155,267,584-155,271,284 , GRCh37.p13 chr6: 155,588,718-155,592,418 TFB1M, CLDN20
    nsv4943547copy number variation1nstd200human GRCh38 chr6: 155,237,316-155,238,397 , GRCh37.p13 chr6: 155,558,450-155,559,531 TIAM2, TFB1M
    nsv4811033copy number variation1nstd200human GRCh37 chr6: 155,600,418-155,603,876 , GRCh38.p12 chr6: 155,279,284-155,282,742 TFB1M
    nsv4811032copy number variation1nstd200human GRCh37 chr6: 155,588,718-155,592,418 , GRCh38.p12 chr6: 155,267,584-155,271,284 TFB1M, CLDN20
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4734969copy number variation1nstd199human GRCh37 chr6: 155,626,292-155,626,365 , GRCh38.p12 chr6: 155,305,158-155,305,231 TFB1M
    nsv4674989copy number variation1nstd102humanUncertain significance GRCh37 chr6: 155,405,078-155,584,960 , GRCh38.p12 chr6: 155,083,944-155,263,826 TIAM2, TFB1M, 1 more genes
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