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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129436insertion1nstd186human GRCh37 chr20: 24,937,719-24,937,745 , GRCh38.p12 chr20: 24,957,083-24,957,109 CST7
    nsv5960629copy number variation1nstd209human GRCh38 chr20: 24,517,514-25,490,454 , GRCh37.p13 chr20: 24,498,150-25,471,090 LOC105372581, LOC107985402, 18 more genes
    nsv5666492insertion1nstd207human GRCh38 chr20: 24,957,078-24,957,078 , GRCh37.p13 chr20: 24,937,714-24,937,714 CST7
    nsv5552113insertion1nstd206human GRCh38 chr20: 24,957,083-24,957,109 , GRCh37.p13 chr20: 24,937,719-24,937,745 CST7
    nsv5529010copy number variation1nstd206human GRCh38 chr20: 24,494,187-25,093,208 , GRCh37.p13 chr20: 24,474,823-25,073,844 CST7, VSX1, 6 more genes
    nsv5025235copy number variation1nstd200human GRCh38 chr20: 24,904,893-24,947,288 , GRCh37.p13 chr20: 24,885,529-24,927,924 LINC02967, CST7
    nsv5025231copy number variation1nstd200human GRCh38 chr20: 24,701,081-24,966,602 , GRCh37.p13 chr20: 24,681,717-24,947,238 LINC02967, LOC107985402, 2 more genes
    nsv5021819copy number variation1nstd200human GRCh38 chr20: 24,953,206-24,955,869 , GRCh37.p13 chr20: 24,933,842-24,936,505 CST7
    nsv5021818copy number variation1nstd200human GRCh38 chr20: 24,946,370-24,948,295 , GRCh37.p13 chr20: 24,927,006-24,928,931 CST7
    nsv4865502copy number variation1nstd200human GRCh37 chr20: 24,885,450-24,927,931 , GRCh38.p12 chr20: 24,904,814-24,947,295 CST7, LINC02967
    nsv4865499copy number variation1nstd200human GRCh37 chr20: 24,681,717-24,947,238 , GRCh38.p12 chr20: 24,701,081-24,966,602 LOC107985402, CST7, 2 more genes
    nsv4862399copy number variation1nstd200human GRCh37 chr20: 24,933,842-24,936,505 , GRCh38.p12 chr20: 24,953,206-24,955,869 CST7
    nsv4761336insertion1nstd199human GRCh37 chr20: 24,937,693-24,937,693 , GRCh38.p12 chr20: 24,957,057-24,957,057 CST7
    nsv4730008copy number variation1nstd102humanUncertain significance GRCh37 chr20: 24,685,850-24,948,039 , GRCh38.p12 chr20: 24,705,214-24,967,403 APMAP, LINC02967, 2 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4628078copy number variation1nstd183human GRCh37 chr20: 24,846,386-25,003,658 , GRCh38.p12 chr20: 24,865,750-25,023,022 RNU6-1257P, CST7, 3 more genes
    nsv4457450copy number variation1nstd102humanUncertain significance GRCh37 chr20: 24,232,978-25,520,939 , GRCh38.p12 chr20: 24,252,342-25,540,303 LOC284798, NINL, 21 more genes
    nsv4442891insertion1nstd175human GRCh37 chr20: 24,937,726-24,937,726 , GRCh38.p12 chr20: 24,957,090-24,957,090 CST7
    nsv4370128copy number variation1nstd173human GRCh37 chr20: 24,880,683-24,932,831 , GRCh38.p12 chr20: 24,900,047-24,952,195 CST7, LINC02967
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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