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Items: 1 to 20 of 455

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114571copy number variation1nstd186human GRCh37 chrX: 10,000,870-10,001,019 , GRCh38.p12 chrX: 10,032,830-10,032,979 WWC3
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980432copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chrX: 8,501,036-11,318,732 , GRCh38.p12 chrX: 8,532,995-11,300,612 FAM9A, NOLC1P1, 23 more genes
    nsv5965026insertion1nstd209human GRCh38 chrX: 10,104,753-10,104,753 , GRCh37.p13 chrX: 10,072,793-10,072,793 WWC3
    nsv5961513insertion1nstd209human GRCh38 chrX: 10,137,110-10,137,110 , GRCh37.p13 chrX: 10,105,150-10,105,150 WWC3
    nsv5882559copy number variation1nstd209human GRCh38 chrX: 10,043,544-10,043,633 , GRCh37.p13 chrX: 10,011,584-10,011,673 WWC3
    nsv5620383insertion1nstd207human GRCh38 chrX: 10,032,830-10,032,830 , GRCh37.p13 chrX: 10,000,870-10,000,870 WWC3
    nsv5608136insertion1nstd207human GRCh38 chrX: 10,137,114-10,137,114 , GRCh37.p13 chrX: 10,105,154-10,105,154 WWC3
    nsv5415380copy number variation1nstd206human GRCh38 chrX: 10,109,324-10,109,407 , GRCh37.p13 chrX: 10,077,364-10,077,447 WWC3
    nsv5414679copy number variation1nstd206human GRCh38 chrX: 10,032,830-10,032,979 , GRCh37.p13 chrX: 10,000,870-10,001,019 WWC3
    nsv5332191translocation1nstd200human GRCh37 chrX: 10,077,447-10,077,447 , GRCh37 chrX: 10,077,364-10,077,364 , GRCh38.p12 chrX: 10,109,324-10,109,324 , GRCh38.p12 chrX: 10,109,407-10,109,407 WWC3
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905185copy number variation1nstd200human GRCh38 chrX: 10,025,036-10,031,140 , GRCh37.p13 chrX: 9,993,076-9,999,180 WWC3
    nsv4905182copy number variation1nstd200human GRCh38 chrX: 9,784,330-10,089,333 , GRCh37.p13 chrX: 9,752,370-10,057,373 , GPR143, 5 more genes
    nsv4772496copy number variation1nstd200human GRCh37 chrX: 9,752,370-10,057,373 , GRCh38.p12 chrX: 9,784,330-10,089,333 , SHROOM2, 5 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4737997insertion1nstd199human GRCh37 chrX: 10,105,098-10,105,098 , GRCh38.p12 chrX: 10,137,058-10,137,058 WWC3
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4728355copy number variation1nstd102humanUncertain significance GRCh37 chrX: 9,751,962-10,054,942 , GRCh38.p12 chrX: 9,783,922-10,086,902 WWC3, GPR143, 4 more genes
    nsv4674815copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-17,502,124 , GRCh38.p12 chrX: 251,879-17,484,001 PTMAP14, LOC100132857, 189 more genes
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