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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946570copy number variation1nstd209human GRCh38 chr18: 25,312,516-25,312,839 , GRCh37.p13 chr18: 22,892,480-22,892,803 ZNF521
    nsv5945138copy number variation1nstd209human GRCh38 chr18: 25,158,189-25,158,850 , GRCh37.p13 chr18: 22,738,153-22,738,814 ZNF521
    nsv5943306copy number variation1nstd209human GRCh38 chr18: 25,084,168-25,084,593 , GRCh37.p13 chr18: 22,664,132-22,664,557 ZNF521
    nsv5941639copy number variation1nstd209human GRCh38 chr18: 25,273,196-25,273,267 , GRCh37.p13 chr18: 22,853,160-22,853,231 ZNF521, LOC105372031
    nsv5939914copy number variation1nstd209human GRCh38 chr18: 25,273,032-25,273,363 , GRCh37.p13 chr18: 22,852,996-22,853,327 LOC105372031, ZNF521
    nsv5730441mobile element insertion2nstd211human GRCh38 chr18: 25,074,615-25,074,615 , GRCh37.p13 chr18: 22,654,579-22,654,579 ZNF521
    nsv5727981mobile element insertion1nstd211human GRCh38 chr18: 25,151,926-25,151,926 , GRCh37.p13 chr18: 22,731,890-22,731,890 ZNF521
    nsv5726270mobile element insertion1nstd211human GRCh38 chr18: 25,346,262-25,346,262 , GRCh37.p13 chr18: 22,926,226-22,926,226 ZNF521
    nsv5723685mobile element insertion1nstd211human GRCh38 chr18: 25,149,677-25,149,677 , GRCh37.p13 chr18: 22,729,641-22,729,641 ZNF521
    nsv5701045mobile element insertion2nstd211human GRCh38 chr18: 25,204,568-25,204,568 , GRCh37.p13 chr18: 22,784,532-22,784,532 ZNF521
    nsv5697924mobile element insertion2nstd211human GRCh38 chr18: 25,084,221-25,084,221 , GRCh37.p13 chr18: 22,664,185-22,664,185 ZNF521
    nsv5695875mobile element insertion2nstd211human GRCh38 chr18: 25,169,165-25,169,165 , GRCh37.p13 chr18: 22,749,129-22,749,129 ZNF521
    nsv5646061insertion1nstd207human GRCh38 chr18: 25,116,877-25,116,877 , GRCh37.p13 chr18: 22,696,841-22,696,841 ZNF521
    nsv5603680copy number variation1nstd207human GRCh38 chr18: 25,312,516-25,312,839 , GRCh37.p13 chr18: 22,892,480-22,892,803 ZNF521
    nsv5602218copy number variation1nstd207human GRCh38 chr18: 25,084,168-25,084,593 , GRCh37.p13 chr18: 22,664,132-22,664,557 ZNF521
    nsv5560415mobile element insertion1nstd206human GRCh38 chr18: 25,149,677-25,149,728 , GRCh37.p13 chr18: 22,729,641-22,729,692 ZNF521
    nsv5559964sequence alteration1nstd206human GRCh37.p13 chr18: 22,445,885-22,922,603 , GRCh38 chr18: 24,865,921-25,342,639 , ZNF521, 4 more genes
    nsv5557963mobile element insertion1nstd206human GRCh38 chr18: 25,346,262-25,346,274 , GRCh37.p13 chr18: 22,926,226-22,926,238 ZNF521
    nsv5544987insertion1nstd206human GRCh38 chr18: 25,338,423-25,338,464 , GRCh37.p13 chr18: 22,918,387-22,918,428 ZNF521
    nsv5542093insertion1nstd206human GRCh38 chr18: 25,306,575-25,306,581 , GRCh37.p13 chr18: 22,886,539-22,886,545 ZNF521
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