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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
    nsv5673916copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,838,632-2,878,441 , GRCh38.p12 chrX: 2,920,591-2,960,400 ARSD, ARSL
    nsv5665780copy number variation1nstd207human GRCh38 chrX: 2,922,845-2,922,897 , GRCh37.p13 chrX: 2,840,886-2,840,938 ARSD
    nsv5664732copy number variation1nstd207human GRCh38 chrX: 2,918,416-2,918,648 , GRCh37.p13 chrX: 2,836,457-2,836,689 ARSD
    nsv5433600copy number variation1nstd206human GRCh38 chrX: 2,921,202-2,921,317 , GRCh37.p13 chrX: 2,839,243-2,839,358 ARSD
    nsv5431814copy number variation1nstd206human GRCh38 chrX: 2,531,036-2,924,507 , GRCh37.p13 chrX: 2,449,077-2,842,548 ARSD, CD99, 7 more genes
    nsv5428336copy number variation1nstd206human GRCh38 chrX: 2,918,421-2,918,649 , GRCh37.p13 chrX: 2,836,462-2,836,690 ARSD
    nsv5426106copy number variation1nstd206human GRCh38 chrX: 2,928,497-2,928,550 , GRCh37.p13 chrX: 2,846,538-2,846,591 ARSD
    nsv5422252copy number variation1nstd206human GRCh38 chrX: 2,655,633-2,992,297 , GRCh37.p13 chrX: 2,573,674-2,910,338 ARSD, ARSL, 5 more genes
    nsv5195182mobile element insertion1nstd203human GRCh38 chrX: 2,918,587-2,918,603 , GRCh37.p13 chrX: 2,836,628-2,836,644 ARSD
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905114copy number variation1nstd200human GRCh38 chrX: 2,760,443-3,265,999 , GRCh37.p13 chrX: 2,678,484-3,184,040 ARSD, XG, 6 more genes
    nsv4905110copy number variation1nstd200human GRCh38 chrX: 2,683,892-3,170,541 , GRCh37.p13 chrX: 2,601,933-3,088,582 ARSL, ARSD, 7 more genes
    nsv4905106copy number variation1nstd200human GRCh38 chrX: 2,472,407-3,562,929 , GRCh37.p13 chrX: 2,390,448-3,480,970 MXRA5, LINC01546, 17 more genes
    nsv4778917copy number variation1nstd200human GRCh37 chrX: 2,831,664-2,832,624 , GRCh38.p12 chrX: 2,913,623-2,914,583 ARSD
    nsv4769315copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-4,857,212 , GRCh38.p12 chrX: 10,001-4,939,171 AKAP17A, RPS27AP20, 58 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728502copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,428,084-3,118,627 , GRCh38.p12 chrX: 2,510,043-3,200,586 CD99, ARSD, 11 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
    nsv4728381copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,571,744-3,605,934 , GRCh38.p12 chrX: 2,653,703-3,687,893 LINC01546, MXRA5, 16 more genes
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