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Items: 1 to 20 of 291

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5936864copy number variation1nstd209human GRCh38 chr19: 36,649,391-36,667,714 , GRCh37.p13 chr19: 37,140,293-37,158,616 ZNF567, ZNF461
    nsv5936559copy number variation1nstd209human GRCh38 chr19: 36,688,242-36,688,668 , GRCh37.p13 chr19: 37,179,144-37,179,570 ZNF567
    nsv5873271copy number variation1nstd209human GRCh38 chr19: 36,652,686-36,667,561 , GRCh37.p13 chr19: 37,143,588-37,158,463 ZNF461, ZNF567
    nsv5709506mobile element insertion1nstd211human GRCh38 chr19: 36,667,615-36,667,615 , GRCh37.p13 chr19: 37,158,517-37,158,517 ZNF567
    nsv5698741mobile element insertion2nstd211human GRCh38 chr19: 36,722,962-36,722,962 , GRCh37.p13 chr19: 37,213,864-37,213,864 ZNF567
    nsv5531446copy number variation1nstd206human GRCh38 chr19: 36,629,204-36,725,597 , GRCh37.p13 chr19: 37,120,106-37,216,499 ZNF461, ZNF567-DT, 2 more genes
    nsv5528459copy number variation1nstd206human GRCh38 chr19: 36,632,408-36,871,986 , GRCh37.p13 chr19: 37,123,310-37,362,888 ZNF345, ZNF382, 7 more genes
    nsv5523075copy number variation1nstd206human GRCh38 chr19: 36,688,534-36,695,251 , GRCh37.p13 chr19: 37,179,436-37,186,153 ZNF567
    nsv5517706copy number variation1nstd206human GRCh38 chr19: 36,688,246-36,688,669 , GRCh37.p13 chr19: 37,179,148-37,179,571 ZNF567
    nsv5516125copy number variation1nstd206human GRCh38 chr19: 36,677,221-36,678,595 , GRCh37.p13 chr19: 37,168,123-37,169,497 ZNF567
    nsv5432332mobile element insertion1nstd206human GRCh38 chr19: 36,722,962-36,723,013 , GRCh37.p13 chr19: 37,213,864-37,213,915 ZNF567
    nsv5377354translocation1nstd200human GRCh38 chr19: 36,667,948-36,667,948 , GRCh38 chr2: 218,292,933-218,292,933 , GRCh37.p13 chr19: 37,158,850-37,158,850 , GRCh37.p13 chr2: 219,157,656-219,157,656 PNKD, TMBIM1, 1 more genes
    nsv5359764translocation1nstd200human GRCh38 chr19: 36,688,669-36,688,669 , GRCh38 chr19: 36,688,246-36,688,246 , GRCh37.p13 chr19: 37,179,148-37,179,148 , GRCh37.p13 chr19: 37,179,571-37,179,571 ZNF567
    nsv5326678copy number variation1nstd204human GRCh38.p13 chr19: 36,632,411-36,871,943 , GRCh37.p13 chr19: 37,123,313-37,362,845 ZNF345, ZNF382, 7 more genes
    nsv5324371copy number variation1nstd204human GRCh38.p13 chr19: 36,682,598-36,692,928 , GRCh37.p13 chr19: 37,173,500-37,183,830 ZNF567-DT, ZNF567
    nsv5293712copy number variation1nstd204human GRCh38.p13 chr19: 36,633,264-36,699,424 , GRCh37.p13 chr19: 37,124,166-37,190,326 ZNF382, ZNF461, 2 more genes
    nsv5290217copy number variation1nstd204human GRCh38.p13 chr19: 36,714,666-36,716,050 , GRCh37.p13 chr19: 37,205,568-37,206,952 ZNF567
    nsv5288797copy number variation1nstd204human GRCh38.p13 chr19: 36,689,501-36,793,400 , GRCh37.p13 chr19: 37,180,403-37,284,302 ZNF850, LOC728485, 1 more genes
    nsv5287579copy number variation1nstd204human GRCh38.p13 chr19: 36,469,001-36,793,700 , GRCh37.p13 chr19: 36,959,903-37,284,602 ZNF260, CTBP2P7, 10 more genes
    nsv5282776copy number variation1nstd204human GRCh38.p13 chr19: 36,708,544-36,721,000 , GRCh37.p13 chr19: 37,199,446-37,211,902 ZNF567
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