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Items: 1 to 20 of 307

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    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
    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
    nsv4674615copy number variation1nstd102humanPathogenic GRCh37 chrX: 1,240,318-20,986,848 , GRCh38.p12 chrX: 1,140,165-20,968,730 RNA5SP499, GS1-600G8.3, 217 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
    nsv4674458copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-34,753,512 , GRCh38.p12 chrX: 251,879-34,735,395 P2RY8, CA5BP1-CA5B, 344 more genes
    nsv4674388copy number variation1nstd102humanLikely benign GRCh37 chrX: 9,895,992-10,348,490 , GRCh38.p12 chrX: 9,927,952-10,380,450 WWC3, CLCN4, 2 more genes
    nsv4674282copy number variation1nstd102humanPathogenic GRCh37 chrX: 537,158-22,883,547 , GRCh38.p12 chrX: 576,423-22,865,430 NHS, EGFL6, 236 more genes
    nsv4674105copy number variation1nstd102humanLikely benign GRCh37 chrX: 9,932,157-10,348,325 , GRCh38.p12 chrX: 9,964,117-10,380,285 WWC3, CLCN4, 1 more genes
    nsv4454842copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,190,434-23,795,839 , GRCh38.p12 chrX: 2,272,393-23,777,722 MBTPS2, LOC101928389, 224 more genes
    nsv4453553copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,703,632-14,129,100 , GRCh38.p12 chrX: 2,785,591-14,110,981 LINC03114, AMELX, 107 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4451246copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-38,054,739 , GRCh38.p12 chrX: 251,879-38,195,486 H3P43, CA5B, 381 more genes
    nsv4450863copy number variation1nstd102humanUncertain significance GRCh37 chrX: 9,751,653-10,057,942 , GRCh38.p12 chrX: 9,783,613-10,089,902 CLDN34, HMGN1P33, 4 more genes
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