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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051301inversion1nstd229human GRCh38 chr4: 70,082,226-70,094,814 , GRCh37.p13 chr4: 70,947,943-70,960,531 CSN1S2AP
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv6754945copy number variation1nstd229human GRCh38 chr4: 70,078,001-70,086,400 , GRCh37.p13 chr4: 70,943,718-70,952,117 CSN1S2AP
    nsv6754154copy number variation1nstd229human GRCh38 chr4: 69,695,734-70,544,125 , GRCh37.p13 chr4: 70,561,452-71,409,842 OPRPN, HTN3, 20 more genes
    nsv6750875copy number variation1nstd229human GRCh38 chr4: 70,044,501-70,144,100 , GRCh37.p13 chr4: 70,910,218-71,009,817 HTN1, CSN1S2BP, 1 more genes
    nsv6748778copy number variation1nstd229human GRCh38 chr4: 69,775,074-70,688,486 , GRCh37.p13 chr4: 70,640,792-71,554,203 SULT1E1, SMR3A, 24 more genes
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6742965copy number variation1nstd229human GRCh38 chr4: 70,060,485-70,070,417 , GRCh37.p13 chr4: 70,926,202-70,936,134 CSN1S2AP
    nsv6741823copy number variation1nstd229human GRCh38 chr4: 70,054,801-70,066,300 , GRCh37.p13 chr4: 70,920,518-70,932,017 CSN1S2AP, HTN1
    nsv6741409copy number variation1nstd229human GRCh38 chr4: 69,753,787-70,216,995 , GRCh37.p13 chr4: 70,619,505-71,082,712 STATH, HTN1, 12 more genes
    nsv6741123copy number variation1nstd229human GRCh38 chr4: 70,065,752-70,068,902 , GRCh37.p13 chr4: 70,931,469-70,934,619 CSN1S2AP
    nsv6636838copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,479,061-70,985,189 , GRCh38.p12 chr4: 69,613,343-70,119,472 HTN3, LOC105377269, 10 more genes
    nsv6636652copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,478,978-70,985,189 , GRCh38.p12 chr4: 69,613,260-70,119,472 CSN1S1, SULT1D1P, 10 more genes
    nsv6629776copy number variation1nstd224human GRCh37 chr4: 70,620,387-71,081,038 , GRCh38.p12 chr4: 69,754,669-70,215,321 , GRCh38.p12 chr4|NW_013171801.1: 1-236,512 CSN2, HTN1, 12 more genes
    nsv6392738copy number variation1nstd223human GRCh38 chr4: 70,084,301-70,085,100 , GRCh37.p13 chr4: 70,950,018-70,950,817 CSN1S2AP
    nsv6390780copy number variation1nstd223human GRCh38 chr4: 70,072,176-70,072,761 , GRCh37.p13 chr4: 70,937,893-70,938,478 CSN1S2AP
    nsv6383205copy number variation1nstd223human GRCh38 chr4: 69,043,346-70,093,612 , GRCh37.p13 chr4: 69,909,064-70,959,329 CSN2, LOC642496, 30 more genes
    nsv6380027copy number variation1nstd223human GRCh38 chr4: 70,074,680-70,075,358 , GRCh37.p13 chr4: 70,940,397-70,941,075 CSN1S2AP
    nsv6380014copy number variation1nstd223human GRCh38 chr4: 70,085,222-70,092,610 , GRCh37.p13 chr4: 70,950,939-70,958,327 CSN1S2AP
    nsv6377534copy number variation1nstd223human GRCh38 chr4: 70,078,813-70,079,445 , GRCh37.p13 chr4: 70,944,530-70,945,162 CSN1S2AP
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