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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
    nsv6116201mobile element insertion1nstd186human GRCh37 chrX: 14,917,236-14,917,236 , GRCh38.p12 chrX: 14,899,114-14,899,114 MOSPD2
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5965875insertion1nstd209human GRCh38 chrX: 14,899,114-14,899,114 , GRCh37.p13 chrX: 14,917,236-14,917,236 MOSPD2
    nsv5718981mobile element insertion2nstd211human GRCh38 chrX: 14,899,131-14,899,131 , GRCh37.p13 chrX: 14,917,253-14,917,253 MOSPD2
    nsv5622965insertion1nstd207human GRCh38 chrX: 14,899,114-14,899,114 , GRCh37.p13 chrX: 14,917,236-14,917,236 MOSPD2
    nsv5557966mobile element insertion1nstd206human GRCh38 chrX: 14,899,114-14,899,114 , GRCh37.p13 chrX: 14,917,236-14,917,236 MOSPD2
    nsv5198725mobile element insertion1nstd203human GRCh38 chrX: 14,899,131-14,899,131 , GRCh37.p13 chrX: 14,917,253-14,917,253 MOSPD2
    nsv5192745mobile element insertion1nstd203human GRCh38 chrX: 14,899,120-14,899,131 , GRCh37.p13 chrX: 14,917,242-14,917,253 MOSPD2
    nsv5188498mobile element insertion1nstd203human GRCh38 chrX: 14,899,113-14,899,131 , GRCh37.p13 chrX: 14,917,235-14,917,253 MOSPD2
    nsv5187599mobile element insertion1nstd203human GRCh38 chrX: 14,899,121-14,899,131 , GRCh37.p13 chrX: 14,917,243-14,917,253 MOSPD2
    nsv5185031mobile element insertion1nstd203human GRCh38 chrX: 14,900,136-14,900,152 , GRCh37.p13 chrX: 14,918,258-14,918,274 MOSPD2
    nsv5183293mobile element insertion1nstd203human GRCh38 chrX: 14,899,114-14,899,130 , GRCh37.p13 chrX: 14,917,236-14,917,252 MOSPD2
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4742333insertion1nstd199human GRCh37 chrX: 14,917,253-14,917,253 , GRCh38.p12 chrX: 14,899,131-14,899,131 MOSPD2
    nsv4728576copy number variation1nstd102humanLikely benign GRCh37 chrX: 14,718,204-15,192,555 , GRCh38.p12 chrX: 14,700,082-15,174,433 GLRA2, NPM1P9, 4 more genes
    nsv4728507copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 10,478,359-15,357,092 , GRCh38.p12 chrX: 10,510,319-15,338,970 AMELX, ARHGAP6, 49 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
    nsv4721690insertion1nstd186human GRCh37 chrX: 14,917,236-14,917,236 , GRCh38.p12 chrX: 14,899,114-14,899,114 MOSPD2
    nsv4686048mobile element insertion1nstd186human GRCh37 chrX: 14,917,253-14,917,253 , GRCh38.p12 chrX: 14,899,131-14,899,131 MOSPD2
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