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Items: 1 to 20 of 374

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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
    nsv5980432copy number variation2nstd102humanPathogenic, Likely benign GRCh37 chrX: 8,501,036-11,318,732 , GRCh38.p12 chrX: 8,532,995-11,300,612 FAM9A, NOLC1P1, 23 more genes
    nsv5876380copy number variation1nstd209human GRCh38 chrX: 10,170,095-10,170,223 , GRCh37.p13 chrX: 10,138,135-10,138,263 CLCN4
    nsv5433591copy number variation1nstd206human GRCh38 chrX: 10,161,154-10,161,920 , GRCh37.p13 chrX: 10,129,194-10,129,960 CLCN4
    nsv5428832copy number variation1nstd206human GRCh38 chrX: 10,215,967-10,216,035 , GRCh37.p13 chrX: 10,184,007-10,184,075 CLCN4
    nsv5366406translocation1nstd200human GRCh38 chrX: 10,217,782-10,217,782 , GRCh38 chrX: 10,217,162-10,217,162 , GRCh37.p13 chrX: 10,185,202-10,185,202 , GRCh37.p13 chrX: 10,185,822-10,185,822 CLCN4
    nsv5338595translocation1nstd200human GRCh37 chrX: 10,166,366-10,166,366 , GRCh37 chrX: 10,166,429-10,166,429 , GRCh38.p12 chrX: 10,198,389-10,198,389 , GRCh38.p12 chrX: 10,198,326-10,198,326 CLCN4
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4893725copy number variation1nstd200human GRCh38 chrX: 10,198,326-10,198,389 , GRCh37.p13 chrX: 10,166,366-10,166,429 CLCN4
    nsv4779070copy number variation1nstd200human GRCh37 chrX: 10,179,042-10,180,193 , GRCh38.p12 chrX: 10,211,002-10,212,153 CLCN4
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4758158copy number variation1nstd199human GRCh37 chrX: 10,143,903-10,143,980 , GRCh38.p12 chrX: 10,175,863-10,175,940 CLCN4
    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
    nsv4674388copy number variation1nstd102humanLikely benign GRCh37 chrX: 9,895,992-10,348,490 , GRCh38.p12 chrX: 9,927,952-10,380,450 WWC3, CLCN4, 2 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
    nsv4674105copy number variation1nstd102humanLikely benign GRCh37 chrX: 9,932,157-10,348,325 , GRCh38.p12 chrX: 9,964,117-10,380,285 WWC3, CLCN4, 1 more genes
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