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Items: 1 to 20 of 348

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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
    nsv5877440copy number variation1nstd209human GRCh38 chrX: 15,370,412-15,377,397 , GRCh37.p13 chrX: 15,388,534-15,395,519 VEGFD, PIR-FIGF
    nsv5431806copy number variation1nstd206human GRCh38 chrX: 15,172,883-15,821,370 , GRCh37.p13 chrX: 15,191,005-15,839,493 , CLTRN, 16 more genes
    nsv5375897translocation1nstd200human GRCh38 chrX: 15,377,398-15,377,398 , GRCh38 chrX: 15,370,413-15,370,413 , GRCh37.p13 chrX: 15,388,535-15,388,535 , GRCh37.p13 chrX: 15,395,520-15,395,520 VEGFD, PIR-FIGF
    nsv5195810mobile element insertion1nstd203human GRCh38 chrX: 15,350,850-15,350,850 , GRCh37.p13 chrX: 15,368,972-15,368,972 VEGFD, PIR-FIGF
    nsv5189248mobile element insertion1nstd203human GRCh38 chrX: 15,351,008-15,351,027 , GRCh37.p13 chrX: 15,369,130-15,369,149 PIR-FIGF, VEGFD
    nsv5181026mobile element insertion1nstd203human GRCh38 chrX: 15,350,844-15,350,844 , GRCh37.p13 chrX: 15,368,966-15,368,966 PIR-FIGF, VEGFD
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905212copy number variation1nstd200human GRCh38 chrX: 15,085,327-15,703,597 , GRCh37.p13 chrX: 15,103,449-15,721,720 , PTMAP14, 14 more genes
    nsv4870062mobile element deletion1nstd200human GRCh37 chrX: 15,369,233-15,369,540 , GRCh38.p12 chrX: 15,351,111-15,351,418 PIR-FIGF, VEGFD
    nsv4779151copy number variation1nstd200human GRCh37 chrX: 15,388,535-15,395,520 , GRCh38.p12 chrX: 15,370,413-15,377,398 PIR-FIGF, VEGFD
    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
    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
    nsv4574599mobile element insertion1nstd166human GRCh37.p13 chrX: 15,398,472-15,398,472 , GRCh38.p12 chrX: 15,380,350-15,380,350 PIR-FIGF, VEGFD
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