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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
    nsv5970029inversion1nstd209human GRCh37.p13 chrX: 15,776,588-15,777,420 , GRCh38 chrX: 15,758,465-15,759,297 CA5B, CA5BP1-CA5B
    nsv5875420copy number variation1nstd209human GRCh38 chrX: 15,767,861-15,773,671 , GRCh37.p13 chrX: 15,785,984-15,791,794 CA5B, CA5BP1-CA5B
    nsv5608071insertion1nstd207human GRCh38 chrX: 15,752,463-15,752,463 , GRCh37.p13 chrX: 15,770,586-15,770,586 CA5B, CA5BP1-CA5B
    nsv5431806copy number variation1nstd206human GRCh38 chrX: 15,172,883-15,821,370 , GRCh37.p13 chrX: 15,191,005-15,839,493 , CLTRN, 16 more genes
    nsv5427333copy number variation1nstd206human GRCh38 chrX: 15,782,749-15,782,879 , GRCh37.p13 chrX: 15,800,872-15,801,002 CA5B, CA5BP1-CA5B
    nsv5421744copy number variation1nstd206human GRCh38 chrX: 15,752,463-15,753,690 , GRCh37.p13 chrX: 15,770,586-15,771,813 CA5B, CA5BP1-CA5B
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4779152copy number variation1nstd200human GRCh37 chrX: 15,776,469-15,782,013 , GRCh38.p12 chrX: 15,758,346-15,763,890 CA5BP1-CA5B, CA5B
    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
    nsv4674815copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-17,502,124 , GRCh38.p12 chrX: 251,879-17,484,001 PTMAP14, LOC100132857, 189 more genes
    nsv4674756copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,674,696-16,049,674 , GRCh38.p12 chrX: 15,656,573-16,031,551 ZRSR2, AP1S2, 7 more genes
    nsv4674687copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,415,636-18,339,030 , GRCh38.p12 chrX: 15,397,514-18,320,910 ZRSR2, HNRNPDLP5, 45 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
    nsv4674415copy number variation1nstd102humanUncertain significance GRCh37 chrX: 15,319,722-16,018,163 , GRCh38.p12 chrX: 15,301,600-16,000,040 AP1S2, CA5B, 17 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
    nsv4574718mobile element insertion1nstd166human GRCh37.p13 chrX: 15,786,679-15,786,679 , GRCh38.p12 chrX: 15,768,556-15,768,556 CA5BP1-CA5B, CA5B
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