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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7014305copy number variation1nstd229human GRCh38 chr19: 9,430,825-9,430,996 , GRCh37.p13 chr19: 9,541,501-9,541,672 ZNF266
    nsv7014217copy number variation1nstd229human GRCh38 chr19: 9,375,901-9,523,100 , GRCh37.p13 chr19: 9,486,577-9,633,776 ZNF266, ZNF426, 7 more genes
    nsv7011931copy number variation1nstd229human GRCh38 chr19: 9,404,571-9,423,787 , GRCh37.p13 chr19: 9,515,247-9,534,463 LOC112268250, ZNF266
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7003177copy number variation1nstd229human GRCh38 chr19: 9,432,224-9,445,712 , GRCh37.p13 chr19: 9,542,900-9,556,388 ZNF266, ZNF560, 1 more genes
    nsv7003176copy number variation1nstd229human GRCh38 chr19: 9,409,511-9,413,341 , GRCh37.p13 chr19: 9,520,187-9,524,017 ZNF266
    nsv6596227inversion1nstd223human GRCh38 chr19: 9,416,514-9,417,247 , GRCh37.p13 chr19: 9,527,190-9,527,923 ZNF266
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5937328copy number variation1nstd209human GRCh38 chr19: 9,417,109-9,417,467 , GRCh37.p13 chr19: 9,527,785-9,528,143 ZNF266
    nsv5875860copy number variation1nstd209human GRCh38 chr19: 9,435,355-9,437,654 , GRCh37.p13 chr19: 9,546,031-9,548,330 ZNF266, LOC105372269
    nsv5523369copy number variation1nstd206human GRCh38 chr19: 9,433,693-9,433,753 , GRCh37.p13 chr19: 9,544,369-9,544,429 ZNF266, LOC105372269
    nsv5515599copy number variation1nstd206human GRCh38 chr19: 9,423,177-9,434,916 , GRCh37.p13 chr19: 9,533,853-9,545,592 ZNF266, LOC105372269
    nsv5359465translocation1nstd200human GRCh38 chr19: 9,417,977-9,417,977 , GRCh38 chr19: 9,418,511-9,418,511 , GRCh37.p13 chr19: 9,529,187-9,529,187 , GRCh37.p13 chr19: 9,528,653-9,528,653 ZNF266
    nsv5321078copy number variation1nstd204human GRCh38.p13 chr19: 9,423,684-9,430,555 , GRCh37.p13 chr19: 9,534,360-9,541,231 ZNF266
    nsv5298613copy number variation1nstd204human GRCh38.p13 chr19: 9,423,401-9,430,500 , GRCh37.p13 chr19: 9,534,077-9,541,176 ZNF266
    nsv5282611copy number variation1nstd204human GRCh38.p13 chr19: 9,423,855-9,430,554 , GRCh37.p13 chr19: 9,534,531-9,541,230 ZNF266
    nsv5166487mobile element insertion1nstd203human GRCh38 chr19: 9,416,463-9,416,507 , GRCh37.p13 chr19: 9,527,139-9,527,183 ZNF266
    nsv4729799copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622 ZNF426-DT, ADAMTS10, 61 more genes
    nsv4457835copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,485,388-9,633,295 , GRCh38.p12 chr19: 9,374,712-9,522,619 ZNF177, ZNF560, 7 more genes

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