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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
    nsv5977569copy number variation2nstd209human GRCh38 chrX: 3,021,776-3,022,816 , GRCh37.p13 chrX: 2,939,817-2,940,857 ARSH
    nsv5970280copy number variation2nstd209human GRCh38 chrX: 3,015,976-3,020,091 , GRCh37.p13 chrX: 2,934,017-2,938,132 ARSH
    nsv5968729copy number variation1nstd209human GRCh38 chrX: 3,023,917-3,036,349 , GRCh37.p13 chrX: 2,941,958-2,954,390 ARSH
    nsv5968147copy number variation1nstd209human GRCh38 chrX: 3,020,637-3,022,816 , GRCh37.p13 chrX: 2,938,678-2,940,857 ARSH
    nsv5967792copy number variation1nstd209human GRCh38 chrX: 3,000,095-3,011,094 , GRCh37.p13 chrX: 2,918,136-2,929,135 ARSH
    nsv5876013copy number variation1nstd209human GRCh38 chrX: 3,016,432-3,019,814 , GRCh37.p13 chrX: 2,934,473-2,937,855 ARSH
    nsv5366345translocation1nstd200human GRCh38 chrX: 3,025,257-3,025,257 , GRCh38 chrX: 3,025,202-3,025,202 , GRCh37.p13 chrX: 2,943,243-2,943,243 , GRCh37.p13 chrX: 2,943,298-2,943,298 ARSH
    nsv5188854mobile element insertion1nstd203human GRCh38 chrX: 3,020,439-3,020,465 , GRCh37.p13 chrX: 2,938,480-2,938,506 ARSH
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5031486inversion1nstd200human GRCh38 chrX: 3,026,618-3,027,832 , GRCh37.p13 chrX: 2,944,659-2,945,873 ARSH
    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
    nsv4778918copy number variation1nstd200human GRCh37 chrX: 2,934,478-2,937,856 , GRCh38.p12 chrX: 3,016,437-3,019,815 ARSH
    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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