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Items: 1 to 20 of 281

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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
    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
    nsv4905298copy number variation1nstd200human GRCh38 chrX: 26,506,342-26,816,878 , GRCh37.p13 chrX: 26,524,459-26,834,995 RNU1-142P, VENTXP8, 3 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
    nsv4674660copy number variation1nstd102humanUncertain significance GRCh37 chrX: 26,746,929-28,039,872 , GRCh38.p12 chrX: 26,728,812-28,021,755 VKORC1P1, DCAF8L1, 15 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
    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
    nsv4370108copy number variation1nstd173human GRCh37 chrX: 13,725,008-29,819,232 , GRCh38.p12 chrX: 13,706,889-29,801,115 , MAGEB6B, 177 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
    nsv3972252copy number variation1nstd102humanLikely benign GRCh37 chrX: 26,525,715-26,812,705 , GRCh38.p12 chrX: 26,507,598-26,794,588 RNU1-142P, VENTXP8, 3 more genes
    nsv3924790copy number variation1nstd102humanUncertain significance NCBI36 chrX: 252,881-154,862,218 , GRCh37.p13 chrX: 332,881-155,209,024 , GRCh38.p12 chrX: 372,146-155,979,359 PA2G4P1, MIR660, 2146 more genes
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