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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945903copy number variation1nstd209human GRCh38 chr12: 96,227,533-96,227,616 , GRCh37.p13 chr12: 96,621,311-96,621,394 ELK3
    nsv5944785copy number variation1nstd209human GRCh38 chr12: 96,226,489-96,226,540 , GRCh37.p13 chr12: 96,620,267-96,620,318 ELK3
    nsv5857404copy number variation1nstd209human GRCh38 chr12: 96,210,400-96,212,417 , GRCh37.p13 chr12: 96,604,178-96,606,195 ELK3
    nsv5600402copy number variation1nstd207human GRCh38 chr12: 96,226,489-96,226,540 , GRCh37.p13 chr12: 96,620,267-96,620,318 ELK3
    nsv5508776copy number variation1nstd206human GRCh38 chr12: 96,213,717-96,213,842 , GRCh37.p13 chr12: 96,607,495-96,607,620 ELK3
    nsv5503490copy number variation1nstd206human GRCh38 chr12: 96,247,415-96,248,073 , GRCh37.p13 chr12: 96,641,193-96,641,851 , ELK3
    nsv5500727copy number variation1nstd206human GRCh38 chr12: 96,215,993-96,220,336 , GRCh37.p13 chr12: 96,609,771-96,614,114 ELK3
    nsv5313592copy number variation1nstd204human GRCh38.p13 chr12: 96,197,041-96,198,379 , GRCh37.p13 chr12: 96,590,819-96,592,157 ELK3
    nsv5262494copy number variation1nstd204human GRCh38.p13 chr12: 96,196,644-96,198,333 , GRCh37.p13 chr12: 96,590,422-96,592,111 ELK3
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995148copy number variation1nstd200human GRCh38 chr12: 96,212,338-96,214,547 , GRCh37.p13 chr12: 96,606,116-96,608,325 ELK3
    nsv4993590copy number variation1nstd200human GRCh38 chr12: 96,133,525-96,560,623 , GRCh37.p13 chr12: 96,527,303-96,954,401 , CDK17, 6 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4845349copy number variation1nstd200human GRCh37 chr12: 96,606,116-96,608,325 , GRCh38.p12 chr12: 96,212,338-96,214,547 ELK3
    nsv4841944copy number variation1nstd200human GRCh37 chr12: 96,656,468-96,656,881 , GRCh38.p12 chr12: 96,262,690-96,263,103 ELK3
    nsv4830063copy number variation1nstd200human GRCh37 chr12: 96,590,829-96,592,156 , GRCh38.p12 chr12: 96,197,051-96,198,378 ELK3
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4615306copy number variation1nstd183human GRCh37 chr12: 96,587,781-96,588,872 , GRCh38.p12 chr12: 96,194,003-96,195,094 ELK3
    nsv4560025sequence alteration1nstd166human GRCh37.p13 chr12: 96,646,391-96,647,096 , GRCh38.p12 chr12: 96,252,613-96,253,318 ELK3
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