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Items: 1 to 20 of 263

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5943968copy number variation1nstd209human GRCh38 chr19: 4,120,853-4,120,946 , GRCh37.p13 chr19: 4,120,851-4,120,944 MAP2K2
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5942301copy number variation1nstd209human GRCh38 chr19: 4,105,503-4,108,466 , GRCh37.p13 chr19: 4,105,501-4,108,464 MAP2K2
    nsv5937927copy number variation1nstd209human GRCh38 chr19: 4,123,554-4,123,605 , GRCh37.p13 chr19: 4,123,551-4,123,602 MAP2K2
    nsv5928479copy number variation1nstd209human GRCh38 chr19: 4,005,350-4,159,439 , GRCh37.p13 chr19: 4,005,348-4,159,436 MAP2K2, ZBTB7A, 2 more genes
    nsv5879879copy number variation1nstd209human GRCh38 chr19: 4,105,563-4,107,462 , GRCh37.p13 chr19: 4,105,561-4,107,460 MAP2K2
    nsv5663471insertion1nstd207human GRCh38 chr19: 4,122,247-4,122,247 , GRCh37.p13 chr19: 4,122,245-4,122,245 MAP2K2
    nsv5663343insertion1nstd207human GRCh38 chr19: 4,122,224-4,122,224 , GRCh37.p13 chr19: 4,122,222-4,122,222 MAP2K2
    nsv5654205insertion1nstd207human GRCh38 chr19: 4,123,554-4,123,554 , GRCh37.p13 chr19: 4,123,551-4,123,551 MAP2K2
    nsv5646792insertion1nstd207human GRCh38 chr19: 4,123,564-4,123,564 , GRCh37.p13 chr19: 4,123,561-4,123,561 MAP2K2
    nsv5521535copy number variation1nstd206human GRCh38 chr19: 4,120,853-4,120,947 , GRCh37.p13 chr19: 4,120,851-4,120,945 MAP2K2
    nsv5515440copy number variation1nstd206human GRCh38 chr19: 4,107,509-4,107,662 , GRCh37.p13 chr19: 4,107,507-4,107,660 MAP2K2
    nsv5381793copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,976,203-4,345,430 , GRCh38.p12 chr19: 3,976,205-4,345,433 MPND, SNORD37, 13 more genes
    nsv5381272copy number variation1nstd102humanUncertain significance GRCh37 chr19: 4,077,097-4,123,882 , GRCh38.p12 chr19: 4,077,099-4,123,885 MAP2K2
    nsv5359410translocation1nstd200human GRCh38 chr19: 4,120,947-4,120,947 , GRCh38 chr19: 4,120,853-4,120,853 , GRCh37.p13 chr19: 4,120,851-4,120,851 , GRCh37.p13 chr19: 4,120,945-4,120,945 MAP2K2
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5290959copy number variation1nstd204human GRCh38.p13 chr19: 3,885,401-4,190,300 , GRCh37.p13 chr19: 3,885,399-4,190,297 PIAS4, ANKRD24, 11 more genes
    nsv5288437copy number variation1nstd204human GRCh38.p13 chr19: 4,121,136-4,123,085 , GRCh37.p13 chr19: 4,121,134-4,123,082 MAP2K2
    nsv5287184copy number variation1nstd204human GRCh38.p13 chr19: 4,121,101-4,123,100 , GRCh37.p13 chr19: 4,121,099-4,123,097 MAP2K2
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