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Items: 1 to 20 of 503

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7077960copy number variation1nstd229human GRCh38 chrX: 10,082,694-10,091,491 , GRCh37.p13 chrX: 10,050,734-10,059,531 WWC3
    nsv7077891copy number variation1nstd229human GRCh38 chrX: 9,959,192-10,074,790 , GRCh37.p13 chrX: 9,927,232-10,042,830 WWC3, CLDN34
    nsv7077610copy number variation1nstd229human GRCh38 chrX: 10,032,830-10,032,965 , GRCh37.p13 chrX: 10,000,870-10,001,005 WWC3
    nsv7075973copy number variation1nstd229human GRCh38 chrX: 9,567,201-10,193,900 , GRCh37.p13 chrX: 9,535,241-10,161,940 CLCN4, LOC105373126, 7 more genes
    nsv7075583copy number variation1nstd229human GRCh38 chrX: 9,670,822-10,136,661 , GRCh37.p13 chrX: 9,638,862-10,104,701 WWC3, GPR143, 6 more genes
    nsv7073933copy number variation1nstd229human GRCh38 chrX: 9,942,920-10,062,403 , GRCh37.p13 chrX: 9,910,960-10,030,443 SHROOM2, WWC3, 1 more genes
    nsv7072943copy number variation1nstd229human GRCh38 chrX: 10,084,401-10,158,700 , GRCh37.p13 chrX: 10,052,441-10,126,740 WWC3, CLCN4
    nsv7069464copy number variation1nstd229human GRCh38 chrX: 9,786,501-10,043,000 , GRCh37.p13 chrX: 9,754,541-10,011,040 HMGN1P33, SHROOM2, 4 more genes
    nsv7069234copy number variation1nstd229human GRCh38 chrX: 9,558,650-10,208,940 , GRCh37.p13 chrX: 9,526,690-10,176,980 CLDN34, SHROOM2, 7 more genes
    nsv7068710copy number variation1nstd229human GRCh38 chrX: 10,109,001-10,109,412 , GRCh37.p13 chrX: 10,077,041-10,077,452 WWC3
    nsv7068469copy number variation1nstd229human GRCh38 chrX: 9,567,301-10,127,700 , GRCh37.p13 chrX: 9,535,341-10,095,740 SHROOM2, HMGN1P33, 6 more genes
    nsv7066920copy number variation1nstd229human GRCh38 chrX: 10,120,501-10,176,000 , GRCh37.p13 chrX: 10,088,541-10,144,040 WWC3, CLCN4
    nsv7065064copy number variation1nstd229human GRCh38 chrX: 10,100,401-10,158,700 , GRCh37.p13 chrX: 10,068,441-10,126,740 CLCN4, WWC3
    nsv7063750copy number variation1nstd229human GRCh38 chrX: 10,069,195-10,069,412 , GRCh37.p13 chrX: 10,037,235-10,037,452 WWC3
    nsv7060828copy number variation1nstd229human GRCh38 chrX: 10,094,101-10,193,900 , GRCh37.p13 chrX: 10,062,141-10,161,940 WWC3, CLCN4
    nsv7060626copy number variation1nstd229human GRCh38 chrX: 10,143,805-10,153,508 , GRCh37.p13 chrX: 10,111,845-10,121,548 WWC3
    nsv7060513copy number variation1nstd229human GRCh38 chrX: 9,784,330-10,089,333 , GRCh37.p13 chrX: 9,752,370-10,057,373 CLDN34, SHROOM2, 4 more genes
    nsv7059539copy number variation1nstd229human GRCh38 chrX: 10,115,801-10,120,600 , GRCh37.p13 chrX: 10,083,841-10,088,640 WWC3
    nsv7034660inversion1nstd229human GRCh38 chrX: 7,485,177-12,037,307 , GRCh37.p13 chrX: 7,403,218-12,055,426 LOC442443, VCX, 37 more genes
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