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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5883181copy number variation1nstd209human GRCh38 chr19: 37,463,204-37,466,329 , GRCh37.p13 chr19: 37,954,106-37,957,231 ZNF570, ZNF569
    nsv5528867copy number variation1nstd206human GRCh38 chr19: 37,425,046-37,425,177 , GRCh37.p13 chr19: 37,915,948-37,916,079 ZNF569
    nsv5525452copy number variation1nstd206human GRCh38 chr19: 37,438,005-37,438,055 , GRCh37.p13 chr19: 37,928,907-37,928,957 ZNF569
    nsv5521146copy number variation1nstd206human GRCh38 chr19: 37,440,215-37,440,679 , GRCh37.p13 chr19: 37,931,117-37,931,581 ZNF569
    nsv5516497copy number variation1nstd206human GRCh38 chr19: 37,467,633-37,640,567 , GRCh37.p13 chr19: 37,958,535-38,131,468 ZNF571-AS1, MTND5P45, 9 more genes
    nsv5328557copy number variation1nstd204human GRCh38.p13 chr19: 37,459,465-37,462,240 , GRCh37.p13 chr19: 37,950,367-37,953,142 ZNF569
    nsv5285304copy number variation1nstd204human GRCh38.p13 chr19: 37,459,204-37,462,153 , GRCh37.p13 chr19: 37,950,106-37,953,055 ZNF569
    nsv5178541mobile element insertion1nstd203human GRCh38 chr19: 37,413,316-37,413,327 , GRCh37.p13 chr19: 37,904,218-37,904,229 ZNF569
    nsv5027816copy number variation1nstd200human GRCh38 chr19: 37,464,416-37,471,213 , GRCh37.p13 chr19: 37,955,318-37,962,115 ZNF570, ZNF569
    nsv5027815copy number variation1nstd200human GRCh38 chr19: 37,455,509-37,455,632 , GRCh37.p13 chr19: 37,946,411-37,946,534 ZNF569
    nsv5027814copy number variation1nstd200human GRCh38 chr19: 37,441,052-37,443,687 , GRCh37.p13 chr19: 37,931,954-37,934,589 ZNF569
    nsv4868252copy number variation1nstd200human GRCh37 chr19: 37,950,394-37,953,121 , GRCh38.p12 chr19: 37,459,492-37,462,219 ZNF569
    nsv4868251copy number variation1nstd200human GRCh37 chr19: 37,931,954-37,934,589 , GRCh38.p12 chr19: 37,441,052-37,443,687 ZNF569
    nsv4729776copy number variation1nstd102humanUncertain significance GRCh37 chr19: 37,820,377-38,083,967 , GRCh38.p12 chr19: 37,329,475-37,593,066 ZNF793-AS1, ZNF569, 10 more genes
    nsv4715509copy number variation1nstd195human GRCh37 chr19: 37,827,901-38,232,451 , GRCh38.p12 chr19: 37,336,999-37,741,550 ZNF527, ZNF540, 15 more genes
    nsv4679943copy number variation1nstd189human GRCh37.p13 chr19: 37,838,926-38,764,481 , GRCh38.p12 chr19: 37,348,024-38,273,841 DPF1, SPINT2, 31 more genes
    nsv4676151copy number variation1nstd102humanLikely benign GRCh37 chr19: 37,820,245-38,150,396 , GRCh38.p12 chr19: 37,329,343-37,659,495 ZNF569, ZNF570, 11 more genes
    nsv4633336copy number variation1nstd183human GRCh37 chr19: 37,950,721-38,260,982 , GRCh38.p12 chr19: 37,459,819-37,770,342 ZNF793-AS1, MTND4P41, 13 more genes
    nsv4627271copy number variation1nstd183human GRCh37 chr19: 37,902,236-37,903,175 , GRCh38.p12 chr19: 37,411,334-37,412,273 ZNF569
    nsv4626591copy number variation2nstd183human GRCh37 chr19: 37,794,850-37,917,542 , GRCh38.p12 chr19: 37,303,948-37,426,640 ZNF527, ZNF569, 1 more genes
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