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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5971393insertion1nstd209human GRCh38 chr19: 16,635,899-16,635,899 , GRCh37.p13 chr19: 16,746,710-16,746,710 SMIM7
    nsv5937644copy number variation1nstd209human GRCh38 chr19: 16,638,218-16,638,272 , GRCh37.p13 chr19: 16,749,029-16,749,083 SMIM7
    nsv5533422copy number variation1nstd206human GRCh38 chr19: 16,638,218-16,638,273 , GRCh37.p13 chr19: 16,749,029-16,749,084 SMIM7
    nsv5524881copy number variation1nstd206human GRCh38 chr19: 16,642,924-16,644,317 , GRCh37.p13 chr19: 16,753,735-16,755,128 SMIM7
    nsv5297696copy number variation1nstd204human GRCh38.p13 chr19: 16,646,626-16,647,725 , GRCh37.p13 chr19: 16,757,437-16,758,536 SMIM7
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5012100copy number variation1nstd200human GRCh38 chr19: 16,639,410-16,641,574 , GRCh37.p13 chr19: 16,750,221-16,752,385 SMIM7
    nsv5012099copy number variation1nstd200human GRCh38 chr19: 16,638,218-16,638,273 , GRCh37.p13 chr19: 16,749,029-16,749,084 SMIM7
    nsv5012098copy number variation1nstd200human GRCh38 chr19: 16,635,704-16,642,342 , GRCh37.p13 chr19: 16,746,515-16,753,153 SMIM7
    nsv5012097copy number variation1nstd200human GRCh38 chr19: 16,633,215-16,634,505 , GRCh37.p13 chr19: 16,744,026-16,745,316 SMIM7
    nsv4860525copy number variation1nstd200human GRCh37 chr19: 16,749,029-16,749,084 , GRCh38.p12 chr19: 16,638,218-16,638,273 SMIM7
    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
    nsv4625430copy number variation1nstd183human GRCh37 chr19: 16,765,698-16,832,596 , GRCh38.p12 chr19: 16,654,887-16,721,785 NWD1, TMEM38A, 1 more genes
    nsv4268509copy number variation1nstd166human GRCh37.p13 chr19: 16,749,029-16,749,084 , GRCh38.p12 chr19: 16,638,218-16,638,273 SMIM7
    nsv4255300copy number variation1nstd166human GRCh37.p13 chr19: 16,766,911-16,776,954 , GRCh38.p12 chr19: 16,656,100-16,666,143 SMIM7, TMEM38A
    nsv4253607copy number variation1nstd166human GRCh37.p13 chr19: 16,741,236-16,742,124 , GRCh38.p12 chr19: 16,630,425-16,631,313 SMIM7
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3916911copy number variation1nstd102humanUncertain significance GRCh37 chr19: 16,595,955-16,783,029 , GRCh38 chr19: 16,485,144-16,672,218 , NCBI36 chr19: 16,456,955-16,644,029 RN7SL146P, CHERP, 8 more genes
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