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Items: 1 to 20 of 568

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7088737copy number variation1nstd229human GRCh38 chrX: 72,148,241-72,155,761 , GRCh37.p13 chrX: 71,368,091-71,375,611 NHSL2
    nsv7088736copy number variation1nstd229human GRCh38 chrX: 72,140,845-72,141,243 , GRCh37.p13 chrX: 71,360,695-71,361,093 NHSL2
    nsv7088735copy number variation1nstd229human GRCh38 chrX: 72,115,437-72,124,247 , GRCh37.p13 chrX: 71,335,287-71,344,097 NHSL2
    nsv7088734copy number variation1nstd229human GRCh38 chrX: 72,101,437-72,106,336 , GRCh37.p13 chrX: 71,321,287-71,326,186 NHSL2
    nsv7088733copy number variation1nstd229human GRCh38 chrX: 72,068,609-72,075,522 , GRCh37.p13 chrX: 71,288,459-71,295,372 NHSL2
    nsv7088732copy number variation1nstd229human GRCh38 chrX: 72,044,201-72,049,500 , GRCh37.p13 chrX: 71,264,051-71,269,350 RPS26P11, NHSL2
    nsv7088731copy number variation1nstd229human GRCh38 chrX: 72,016,148-72,016,354 , GRCh37.p13 chrX: 71,235,998-71,236,204 NHSL2
    nsv7088730copy number variation1nstd229human GRCh38 chrX: 72,011,458-72,011,665 , GRCh37.p13 chrX: 71,231,308-71,231,515 NHSL2
    nsv7088729copy number variation1nstd229human GRCh38 chrX: 72,003,801-72,012,500 , GRCh37.p13 chrX: 71,223,651-71,232,350 NHSL2
    nsv7088728copy number variation1nstd229human GRCh38 chrX: 71,974,391-71,974,857 , GRCh37.p13 chrX: 71,194,241-71,194,707 NHSL2
    nsv7088727copy number variation1nstd229human GRCh38 chrX: 71,965,532-71,965,693 , GRCh37.p13 chrX: 71,185,382-71,185,543 RNU6-1078P, NHSL2
    nsv7088726copy number variation1nstd229human GRCh38 chrX: 71,965,526-71,965,694 , GRCh37.p13 chrX: 71,185,376-71,185,544 NHSL2, RNU6-1078P
    nsv7088725copy number variation1nstd229human GRCh38 chrX: 71,951,900-71,952,073 , GRCh37.p13 chrX: 71,171,750-71,171,923 NHSL2
    nsv7088724copy number variation1nstd229human GRCh38 chrX: 71,941,829-72,060,461 , GRCh37.p13 chrX: 71,161,679-71,280,311 RPS26P11, RNU6-1078P, 1 more genes
    nsv7088723copy number variation1nstd229human GRCh38 chrX: 71,938,501-71,955,500 , GRCh37.p13 chrX: 71,158,351-71,175,350 NHSL2
    nsv7088722copy number variation1nstd229human GRCh38 chrX: 71,917,506-71,921,087 , GRCh37.p13 chrX: 71,137,356-71,140,937 NHSL2
    nsv7088721copy number variation1nstd229human GRCh38 chrX: 71,908,999-71,909,225 , GRCh37.p13 chrX: 71,128,849-71,129,075 NHSL2
    nsv7032661inversion1nstd229human GRCh38 chrX: 72,007,699-72,012,502 , GRCh37.p13 chrX: 71,227,549-71,232,352 NHSL2
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