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Items: 1 to 20 of 354

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926232copy number variation1nstd209human GRCh38 chr11: 120,415,325-120,415,394 , GRCh37.p13 chr11: 120,286,034-120,286,103 ARHGEF12
    nsv5921883copy number variation1nstd209human GRCh38 chr11: 120,450,769-120,450,925 , GRCh37.p13 chr11: 120,321,478-120,321,634 ARHGEF12
    nsv5851006copy number variation1nstd209human GRCh38 chr11: 120,378,568-120,379,567 , GRCh37.p13 chr11: 120,249,277-120,250,276 ARHGEF12
    nsv5713603mobile element insertion1nstd211human GRCh38 chr11: 120,469,067-120,469,067 , GRCh37.p13 chr11: 120,339,776-120,339,776 ARHGEF12
    nsv5709553mobile element insertion2nstd211human GRCh38 chr11: 120,372,648-120,372,648 , GRCh37.p13 chr11: 120,243,357-120,243,357 ARHGEF12
    nsv5707224mobile element insertion2nstd211human GRCh38 chr11: 120,420,361-120,420,361 , GRCh37.p13 chr11: 120,291,070-120,291,070 ARHGEF12
    nsv5694922mobile element insertion1nstd211human GRCh38 chr11: 120,351,424-120,351,424 , GRCh37.p13 chr11: 120,222,133-120,222,133 ARHGEF12
    nsv5645601insertion1nstd207human GRCh38 chr11: 120,420,344-120,420,344 , GRCh37.p13 chr11: 120,291,053-120,291,053 ARHGEF12
    nsv5511090copy number variation1nstd206human GRCh38 chr11: 120,357,624-120,359,474 , GRCh37.p13 chr11: 120,228,333-120,230,183 ARHGEF12
    nsv5506819copy number variation1nstd206human GRCh38 chr11: 120,485,289-120,485,509 , GRCh37.p13 chr11: 120,355,998-120,356,218 ARHGEF12
    nsv5503379copy number variation1nstd206human GRCh38 chr11: 120,450,769-120,450,927 , GRCh37.p13 chr11: 120,321,478-120,321,636 ARHGEF12
    nsv5501867copy number variation1nstd206human GRCh38 chr11: 120,482,007-120,483,882 , GRCh37.p13 chr11: 120,352,716-120,354,591 ARHGEF12
    nsv5430871mobile element insertion1nstd206human GRCh38 chr11: 120,420,361-120,420,412 , GRCh37.p13 chr11: 120,291,070-120,291,121 ARHGEF12
    nsv5422020mobile element insertion1nstd206human GRCh38 chr11: 120,372,648-120,372,699 , GRCh37.p13 chr11: 120,243,357-120,243,408 ARHGEF12
    nsv5420864mobile element insertion1nstd206human GRCh38 chr11: 120,469,067-120,469,118 , GRCh37.p13 chr11: 120,339,776-120,339,827 ARHGEF12
    nsv5373891translocation1nstd200human GRCh38 chr11: 120,359,472-120,359,472 , GRCh38 chr11: 120,357,856-120,357,856 , GRCh37.p13 chr11: 120,228,565-120,228,565 , GRCh37.p13 chr11: 120,230,181-120,230,181 ARHGEF12
    nsv5348367translocation1nstd200human GRCh38 chr11: 120,399,442-120,399,442 , GRCh38 chr11: 120,399,554-120,399,554 , GRCh37.p13 chr11: 120,270,151-120,270,151 , GRCh37.p13 chr11: 120,270,263-120,270,263 ARHGEF12
    nsv5332129translocation1nstd200human GRCh37 chr11: 120,230,181-120,230,181 , GRCh37 chr11: 120,228,566-120,228,566 , GRCh38.p12 chr11: 120,357,857-120,357,857 , GRCh38.p12 chr11: 120,359,472-120,359,472 ARHGEF12
    nsv5330499translocation1nstd200human GRCh37 chr11: 120,286,034-120,286,034 , GRCh37 chr11: 120,286,104-120,286,104 , GRCh38.p12 chr11: 120,415,325-120,415,325 , GRCh38.p12 chr11: 120,415,395-120,415,395 ARHGEF12
    nsv5316173copy number variation1nstd204human GRCh38.p13 chr11: 120,450,763-120,450,935 , GRCh37.p13 chr11: 120,321,472-120,321,644 ARHGEF12
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