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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125845copy number variation1nstd186human GRCh37 chr22: 38,625,615-38,626,242 , GRCh38.p12 chr22: 38,229,609-38,230,236 TMEM184B, RN7SL704P
    nsv5961457copy number variation1nstd209human GRCh38 chr22: 38,229,609-38,230,235 , GRCh37.p13 chr22: 38,625,615-38,626,241 RN7SL704P, TMEM184B
    nsv5955082copy number variation1nstd209human GRCh38 chr22: 38,255,271-38,255,418 , GRCh37.p13 chr22: 38,651,277-38,651,424 TMEM184B
    nsv5665790insertion2nstd207human GRCh38 chr22: 38,229,931-38,229,931 , GRCh37.p13 chr22: 38,625,937-38,625,937 TMEM184B, RN7SL704P
    nsv5664866insertion1nstd207human GRCh38 chr22: 38,230,186-38,230,186 , GRCh37.p13 chr22: 38,626,192-38,626,192 RN7SL704P, TMEM184B
    nsv5599522copy number variation1nstd207human GRCh38 chr22: 38,245,608-38,245,668 , GRCh37.p13 chr22: 38,641,614-38,641,674 TMEM184B
    nsv5599031copy number variation1nstd207human GRCh38 chr22: 38,245,257-38,245,378 , GRCh37.p13 chr22: 38,641,263-38,641,384 TMEM184B
    nsv5595243copy number variation1nstd207human GRCh38 chr22: 38,229,931-38,229,987 , GRCh37.p13 chr22: 38,625,937-38,625,993 TMEM184B, RN7SL704P
    nsv5593512copy number variation1nstd207human GRCh38 chr22: 38,229,703-38,229,816 , GRCh37.p13 chr22: 38,625,709-38,625,822 TMEM184B, RN7SL704P
    nsv5592212copy number variation1nstd207human GRCh38 chr22: 38,229,646-38,229,930 , GRCh37.p13 chr22: 38,625,652-38,625,936 RN7SL704P, TMEM184B
    nsv5585770copy number variation1nstd207human GRCh38 chr22: 38,217,260-38,217,415 , GRCh37.p13 chr22: 38,613,267-38,613,422 TMEM184B
    nsv5551201copy number variation1nstd206human GRCh38 chr22: 38,259,919-38,267,533 , GRCh37.p13 chr22: 38,655,925-38,663,539 TMEM184B
    nsv5546186copy number variation1nstd206human GRCh38 chr22: 38,193,358-38,217,372 , GRCh37.p13 chr22: 38,589,365-38,613,379 MAFF, TMEM184B
    nsv5534765copy number variation1nstd206human GRCh38 chr22: 38,229,609-38,230,236 , GRCh37.p13 chr22: 38,625,615-38,626,242 TMEM184B, RN7SL704P
    nsv5326301copy number variation1nstd204human GRCh37.p13 chr22: 38,625,591-38,626,263 , GRCh38.p13 chr22: 38,229,585-38,230,257 TMEM184B, RN7SL704P
    nsv5295103copy number variation1nstd204human GRCh38.p13 chr22: 38,189,301-38,287,800 , GRCh37.p13 chr22: 38,585,308-38,683,806 RN7SL704P, MAFF, 2 more genes
    nsv5160325mobile element insertion1nstd203human GRCh38 chr22: 38,241,883-38,241,907 , GRCh37.p13 chr22: 38,637,889-38,637,913 TMEM184B
    nsv5041102copy number variation1nstd200human GRCh38 chr22: 38,193,306-38,217,501 , GRCh37.p13 chr22: 38,589,313-38,613,508 MAFF, TMEM184B
    nsv5038962copy number variation1nstd200human GRCh38 chr22: 38,221,784-38,223,666 , GRCh37.p13 chr22: 38,617,791-38,619,673 SNORA92, TMEM184B
    nsv5037405copy number variation1nstd200human GRCh38 chr22: 38,207,402-38,222,649 , GRCh37.p13 chr22: 38,603,409-38,618,656 MAFF, SNORA92, 1 more genes
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