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Items: 1 to 20 of 439

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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
    nsv5978245copy number variation1nstd209human GRCh38 chrX: 2,946,041-2,947,482 , GRCh37.p13 chrX: 2,864,082-2,865,523 ARSL
    nsv5883559copy number variation1nstd209human GRCh38 chrX: 2,952,216-2,952,314 , GRCh37.p13 chrX: 2,870,257-2,870,355 ARSL
    nsv5673916copy number variation1nstd102humanPathogenic GRCh37 chrX: 2,838,632-2,878,441 , GRCh38.p12 chrX: 2,920,591-2,960,400 ARSD, ARSL
    nsv5620434insertion1nstd207human GRCh38 chrX: 2,966,914-2,966,914 , GRCh37.p13 chrX: 2,884,955-2,884,955 ARSL
    nsv5424852copy number variation1nstd206human GRCh38 chrX: 2,966,914-2,967,009 , GRCh37.p13 chrX: 2,884,955-2,885,050 ARSL
    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
    nsv5196178mobile element insertion1nstd203human GRCh38 chrX: 2,960,268-2,960,294 , GRCh37.p13 chrX: 2,878,309-2,878,335 ARSL
    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
    nsv4772454copy number variation1nstd200human GRCh37 chrX: 2,875,502-2,883,476 , GRCh38.p12 chrX: 2,957,461-2,965,435 ARSL
    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
    nsv4728135copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,422,650-2,965,166 , GRCh38.p12 chrX: 2,504,609-3,047,125 XG, MIR6089, 10 more genes
    nsv4685941copy number variation1nstd102humanUncertain significance GRCh37 chrX: 2,748,537-2,937,367 , GRCh38.p12 chrX: 2,830,496-3,019,326 ARSL, GYG2, 3 more genes
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