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Items: 1 to 20 of 292

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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
    nsv5674090copy number variation1nstd102humanPathogenic GRCh37 chrX: 27,765,013-31,697,703 , GRCh38.p12 chrX: 27,746,896-31,679,586 LOC392436, MAGEB2, 32 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4779369copy number variation1nstd200human GRCh37 chrX: 28,032,402-31,547,205 , GRCh38.p12 chrX: 28,014,285-31,529,088 RNA5SP500, FTHL17, 24 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
    nsv4728468copy number variation1nstd102humanPathogenic GRCh37 chrX: 28,309,706-31,853,992 , GRCh38.p12 chrX: 28,291,589-31,835,875 MAGEB1, MAGEB4, 22 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
    nsv4452894copy number variation1nstd102humannot provided GRCh37 chrX: 27,346,252-33,328,836 , GRCh38.p12 chrX: 27,328,135-33,310,719 PTP4A1P5, MAGEB3, 42 more genes
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4451942copy number variation1nstd102humanPathogenic GRCh37 chrX: 20,925,922-35,511,818 , GRCh38.p12 chrX: 20,907,804-35,493,701 LOC100420245, SNRPEP9, 117 more genes
    nsv4451246copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-38,054,739 , GRCh38.p12 chrX: 251,879-38,195,486 H3P43, CA5B, 381 more genes
    nsv4436319copy number variation1nstd102humanPathogenic GRCh37 chrX: 1-47,140,860 , GRCh38.p12 chrX: 10,001-47,281,461 RNU6-266P, MID1IP1, 515 more genes
    nsv4436196copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,814-50,519,984 , GRCh38.p12 chrX: 10,814-50,776,984 CTPS2, CLTRN, 653 more genes
    nsv4380296copy number variation3nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , RPL31P63, 2192 more genes
    nsv4372931copy number variation1nstd173human GRCh37 chrX: 24,512,595-31,458,625 , GRCh38.p12 chrX: 24,494,478-31,440,508 RNU1-142P, CKS1BP6, 68 more genes
    nsv4371363copy number variation1nstd173human GRCh37 chrX: 29,819,249-32,873,718 , GRCh38.p12 chrX: 29,801,132-32,855,601 LOC107985632, FTLP2, 22 more genes
    nsv4367211copy number variation1nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , MIR421, 2192 more genes
    nsv4354951copy number variation1nstd102humanPathogenic GRCh37 chrX: 15,323,210-153,542,100 , GRCh38.p12 chrX: 15,305,088-154,313,750 OR5BH1P, H2BP8, 1929 more genes
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