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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
    nsv5564483copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,712,079-24,839,720 , GRCh38.p12 chrX: 24,693,962-24,821,603 EEF1B2P3, SCARNA23, 1 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
    nsv4905286copy number variation1nstd200human GRCh38 chrX: 24,678,044-24,866,604 , GRCh37.p13 chrX: 24,696,161-24,884,721 POLA1, EEF1B2P3, 2 more genes
    nsv4905285copy number variation1nstd200human GRCh38 chrX: 24,585,705-25,343,040 , GRCh37.p13 chrX: 24,603,822-25,361,157 RN7SL91P, H2BP7, 9 more genes
    nsv4781894copy number variation1nstd200human GRCh37 chrX: 24,603,822-25,361,157 , GRCh38.p12 chrX: 24,585,705-25,343,040 EEF1B2P3, PCYT1B, 9 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
    nsv4728343copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,687,736-25,563,452 , GRCh38.p12 chrX: 24,669,619-25,545,335 SCARNA23, PCYT1B, 8 more genes
    nsv4728297copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,466,056-24,968,754 , GRCh38.p12 chrX: 24,447,939-24,950,637 PCYT1B-AS1, LOC100288233, 7 more genes
    nsv4728234copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,633,853-24,860,330 , GRCh38.p12 chrX: 24,615,736-24,842,213 EEF1B2P3, POLA1, 5 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
    nsv4450939copy number variation1nstd102humanUncertain significance GRCh37 chrX: 24,619,903-25,140,021 , GRCh38.p12 chrX: 24,601,786-25,121,904 ARX, PAFAH1B2P1, 8 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
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