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Items: 1 to 20 of 455

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975777insertion1nstd209human GRCh38 chr13: 97,329,640-97,329,640 , GRCh37.p13 chr13: 97,981,894-97,981,894 MBNL2
    nsv5969247insertion1nstd209human GRCh38 chr13: 97,291,900-97,291,900 , GRCh37.p13 chr13: 97,944,154-97,944,154 MBNL2, LOC101927385
    nsv5945050copy number variation1nstd209human GRCh38 chr13: 97,372,305-97,372,409 , GRCh37.p13 chr13: 98,024,559-98,024,663 MBNL2
    nsv5929394copy number variation1nstd209human GRCh38 chr13: 97,289,400-97,291,911 , GRCh37.p13 chr13: 97,941,654-97,944,165 LOC101927385, MBNL2
    nsv5862568copy number variation1nstd209human GRCh38 chr13: 97,289,311-97,291,765 , GRCh37.p13 chr13: 97,941,565-97,944,019 LOC101927385, MBNL2
    nsv5728435mobile element insertion1nstd211human GRCh38 chr13: 97,266,494-97,266,494 , GRCh37.p13 chr13: 97,918,748-97,918,748 LOC101927385, MBNL2
    nsv5701824mobile element insertion1nstd211human GRCh38 chr13: 97,285,777-97,285,777 , GRCh37.p13 chr13: 97,938,031-97,938,031 LOC101927385, MBNL2
    nsv5695945mobile element insertion1nstd211human GRCh38 chr13: 97,285,774-97,285,774 , GRCh37.p13 chr13: 97,938,028-97,938,028 LOC101927385, MBNL2
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5661940insertion1nstd207human GRCh38 chr13: 97,339,102-97,339,102 , GRCh37.p13 chr13: 97,991,356-97,991,356 MBNL2
    nsv5655004insertion1nstd207human GRCh38 chr13: 97,329,640-97,329,640 , GRCh37.p13 chr13: 97,981,894-97,981,894 MBNL2
    nsv5651263insertion1nstd207human GRCh38 chr13: 97,329,726-97,329,726 , GRCh37.p13 chr13: 97,981,980-97,981,980 MBNL2
    nsv5645367insertion1nstd207human GRCh38 chr13: 97,378,122-97,378,122 , GRCh37.p13 chr13: 98,030,376-98,030,376 MBNL2
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5555497mobile element insertion1nstd206human GRCh38 chr13: 97,266,494-97,266,545 , GRCh37.p13 chr13: 97,918,748-97,918,799 MBNL2, LOC101927385
    nsv5545572insertion1nstd206human GRCh38 chr13: 97,349,449-97,349,449 , GRCh37.p13 chr13: 98,001,703-98,001,703 MBNL2
    nsv5540454insertion1nstd206human GRCh38 chr13: 97,285,777-97,285,813 , GRCh37.p13 chr13: 97,938,031-97,938,067 MBNL2, LOC101927385
    nsv5512542copy number variation1nstd206human GRCh38 chr13: 97,289,404-97,291,912 , GRCh37.p13 chr13: 97,941,658-97,944,166 MBNL2, LOC101927385
    nsv5498038copy number variation1nstd206human GRCh38 chr13: 97,262,908-97,263,051 , GRCh37.p13 chr13: 97,915,162-97,915,305 LOC101927385, MBNL2
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