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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124942copy number variation1nstd186human GRCh37 chr19: 18,044,854-18,045,157 , GRCh38.p12 chr19: 17,934,045-17,934,348 CCDC124
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5943020copy number variation1nstd209human GRCh38 chr19: 17,934,045-17,934,334 , GRCh37.p13 chr19: 18,044,854-18,045,143 CCDC124
    nsv5932879copy number variation1nstd209human GRCh38 chr19: 17,934,342-17,934,738 , GRCh37.p13 chr19: 18,045,151-18,045,547 CCDC124
    nsv5596909copy number variation1nstd207human GRCh38 chr19: 17,934,048-17,934,339 , GRCh37.p13 chr19: 18,044,857-18,045,148 CCDC124
    nsv5518463copy number variation1nstd206human GRCh38 chr19: 17,934,045-17,934,348 , GRCh37.p13 chr19: 18,044,854-18,045,157 CCDC124
    nsv5359546translocation1nstd200human GRCh38 chr19: 17,934,348-17,934,348 , GRCh38 chr19: 17,934,045-17,934,045 , GRCh37.p13 chr19: 18,044,854-18,044,854 , GRCh37.p13 chr19: 18,045,157-18,045,157 CCDC124
    nsv5330844translocation1nstd200human GRCh37 chr19: 18,045,157-18,045,157 , GRCh37 chr19: 18,044,854-18,044,854 , GRCh38.p12 chr19: 17,934,045-17,934,045 , GRCh38.p12 chr19: 17,934,348-17,934,348 CCDC124
    nsv5326091translocation1nstd204human GRCh38.p13 chr19: 17,934,045-17,934,045 , GRCh38.p13 chr19: 17,934,348-17,934,348 , GRCh37.p13 chr19: 18,044,854-18,044,854 , GRCh37.p13 chr19: 18,045,157-18,045,157 CCDC124
    nsv5325844copy number variation1nstd204human GRCh38.p13 chr19: 17,940,951-17,945,120 , GRCh37.p13 chr19: 18,051,760-18,055,929 CCDC124
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5288542copy number variation1nstd204human GRCh38.p13 chr19: 17,940,505-17,944,769 , GRCh37.p13 chr19: 18,051,314-18,055,578 CCDC124
    nsv5170065mobile element insertion1nstd203human GRCh38 chr19: 17,931,048-17,931,075 , GRCh37.p13 chr19: 18,041,857-18,041,884 CCDC124
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014631copy number variation1nstd200human GRCh38 chr19: 17,941,180-17,944,927 , GRCh37.p13 chr19: 18,051,989-18,055,736 CCDC124
    nsv5014629copy number variation1nstd200human GRCh38 chr19: 17,862,333-17,966,738 , GRCh37.p13 chr19: 17,973,142-18,077,547 CCDC124, SNORA68, 3 more genes
    nsv4864987copy number variation1nstd200human GRCh37 chr19: 18,051,989-18,055,736 , GRCh38.p12 chr19: 17,941,180-17,944,927 CCDC124
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4646636copy number variation1nstd186human GRCh37 chr19: 18,044,854-18,045,355 , GRCh38.p12 chr19: 17,934,045-17,934,546 CCDC124
    nsv4618826copy number variation1nstd183human GRCh37 chr19: 18,042,337-18,057,197 , GRCh38.p12 chr19: 17,931,528-17,946,388 CCDC124
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