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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
    nsv5720373mobile element insertion2nstd211human GRCh38 chrX: 15,552,660-15,552,660 , GRCh37.p13 chrX: 15,570,783-15,570,783 BMX, ACE2
    nsv5559274mobile element insertion1nstd206human GRCh38 chrX: 15,552,660-15,552,711 , GRCh37.p13 chrX: 15,570,783-15,570,834 ACE2, BMX
    nsv5431806copy number variation1nstd206human GRCh38 chrX: 15,172,883-15,821,370 , GRCh37.p13 chrX: 15,191,005-15,839,493 , CLTRN, 16 more genes
    nsv5428757copy number variation1nstd206human GRCh38 chrX: 15,504,398-15,558,769 , GRCh37.p13 chrX: 15,522,521-15,576,892 ACE2, BMX, 1 more genes
    nsv5192507mobile element insertion1nstd203human GRCh38 chrX: 15,552,647-15,552,660 , GRCh37.p13 chrX: 15,570,770-15,570,783 ACE2, BMX
    nsv5172563mobile element insertion1nstd203human GRCh38 chrX: 15,510,226-15,510,234 , GRCh37.p13 chrX: 15,528,349-15,528,357 ACE2, BMX
    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
    nsv4902495copy number variation1nstd200human GRCh38 chrX: 15,521,602-15,521,758 , GRCh37.p13 chrX: 15,539,725-15,539,881 ACE2, BMX
    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
    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
    nsv4574080mobile element insertion1nstd166human GRCh37.p13 chrX: 15,570,770-15,570,770 , GRCh38.p12 chrX: 15,552,647-15,552,647 BMX, ACE2
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