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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
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5975678copy number variation1nstd209human GRCh38 chrX: 141,849,653-141,861,514 , GRCh37.p13 chrX: 140,937,439-140,949,300 MAGEC3
    nsv5969600copy number variation2nstd209human GRCh38 chrX: 141,881,501-141,888,100 , GRCh37.p13 chrX: 140,969,287-140,975,886 MAGEC3
    nsv5882095copy number variation1nstd209human GRCh38 chrX: 141,851,196-142,041,663 , GRCh37.p13 chrX: 140,938,982-141,129,449 MAGEC1, MAGEC3
    nsv5868548copy number variation1nstd209human GRCh38 chrX: 141,895,521-141,896,350 , GRCh37.p13 chrX: 140,983,307-140,984,136 MAGEC3
    nsv5426924copy number variation1nstd206human GRCh38 chrX: 141,869,960-141,871,644 , GRCh37.p13 chrX: 140,957,746-140,959,430 MAGEC3
    nsv5424557copy number variation1nstd206human GRCh38 chrX: 141,880,600-141,896,000 , GRCh37.p13 chrX: 140,968,386-140,983,786 MAGEC3
    nsv5419988copy number variation1nstd206human GRCh38 chrX: 141,869,384-141,870,764 , GRCh37.p13 chrX: 140,957,170-140,958,550 MAGEC3
    nsv5377185translocation1nstd200human GRCh38 chrX: 141,869,960-141,869,960 , GRCh38 chrX: 141,871,644-141,871,644 , GRCh37.p13 chrX: 140,959,430-140,959,430 , GRCh37.p13 chrX: 140,957,746-140,957,746 MAGEC3
    nsv5377184translocation1nstd200human GRCh38 chrX: 141,858,424-141,858,424 , GRCh38 chrX: 141,863,564-141,863,564 , GRCh37.p13 chrX: 140,946,210-140,946,210 , GRCh37.p13 chrX: 140,951,350-140,951,350 MAGEC3
    nsv5344875translocation1nstd200human GRCh37 chrX: 140,959,430-140,959,430 , GRCh37 chrX: 140,957,746-140,957,746 , GRCh38.p12 chrX: 141,871,644-141,871,644 , GRCh38.p12 chrX: 141,869,960-141,869,960 MAGEC3
    nsv5332378translocation1nstd200human GRCh37 chrX: 140,979,434-140,979,434 , GRCh37 chrX: 140,979,511-140,979,511 , GRCh38.p12 chrX: 141,891,648-141,891,648 , GRCh38.p12 chrX: 141,891,725-141,891,725 MAGEC3
    nsv5193243mobile element insertion1nstd203human GRCh38 chrX: 141,847,406-141,847,421 , GRCh37.p13 chrX: 140,935,192-140,935,207 MAGEC3
    nsv5190711mobile element insertion1nstd203human GRCh38 chrX: 141,876,822-141,876,845 , GRCh37.p13 chrX: 140,964,608-140,964,631 MAGEC3
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4782394copy number variation1nstd200human GRCh37 chrX: 140,938,982-141,129,452 , GRCh38.p12 chrX: 141,851,196-142,041,666 MAGEC3, MAGEC1
    nsv4782388copy number variation1nstd200human GRCh37 chrX: 139,997,371-140,939,946 , GRCh38.p12 chrX: 140,915,206-141,852,160 SPANXA1, RNU6-3P, 12 more genes
    nsv4780621copy number variation1nstd200human GRCh37 chrX: 140,954,245-140,954,953 , GRCh38.p12 chrX: 141,866,459-141,867,167 MAGEC3
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
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