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Items: 1 to 20 of 947

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145191insertion1nstd232human GRCh37.p13 chrX: 5,913,072-5,913,072 , GRCh38.p12 chrX: 5,995,031-5,995,031 NLGN4X
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv7077152copy number variation1nstd229human GRCh38 chrX: 6,051,643-6,446,918 , GRCh37.p13 chrX: 5,969,684-6,364,959 MIR4770, LOC105373156, 2 more genes
    nsv7077099copy number variation1nstd229human GRCh38 chrX: 6,162,907-6,204,920 , GRCh37.p13 chrX: 6,080,948-6,122,961 NLGN4X
    nsv7076173copy number variation1nstd229human GRCh38 chrX: 6,218,213-6,874,209 , GRCh37.p13 chrX: 6,136,254-6,792,250 LOC105373156, NLGN4X, 4 more genes
    nsv7075019copy number variation1nstd229human GRCh38 chrX: 6,114,458-6,117,490 , GRCh37.p13 chrX: 6,032,499-6,035,531 NLGN4X
    nsv7074143copy number variation1nstd229human GRCh38 chrX: 5,906,838-5,910,548 , GRCh37.p13 chrX: 5,824,879-5,828,589 NLGN4X
    nsv7074096copy number variation1nstd229human GRCh38 chrX: 5,819,401-6,170,100 , GRCh37.p13 chrX: 5,737,442-6,088,141 NLGN4X
    nsv7073967copy number variation1nstd229human GRCh38 chrX: 5,893,705-5,893,992 , GRCh37.p13 chrX: 5,811,746-5,812,033 NLGN4X
    nsv7073037copy number variation1nstd229human GRCh38 chrX: 6,178,732-6,179,343 , GRCh37.p13 chrX: 6,096,773-6,097,384 NLGN4X
    nsv7072952copy number variation1nstd229human GRCh38 chrX: 6,071,276-6,074,796 , GRCh37.p13 chrX: 5,989,317-5,992,837 NLGN4X
    nsv7072685copy number variation1nstd229human GRCh38 chrX: 5,879,689-6,060,173 , GRCh37.p13 chrX: 5,797,730-5,978,214 NLGN4X
    nsv7071015copy number variation1nstd229human GRCh38 chrX: 6,074,154-6,074,344 , GRCh37.p13 chrX: 5,992,195-5,992,385 NLGN4X
    nsv7071011copy number variation1nstd229human GRCh38 chrX: 6,190,517-6,190,697 , GRCh37.p13 chrX: 6,108,558-6,108,738 NLGN4X
    nsv7070423copy number variation1nstd229human GRCh38 chrX: 6,055,550-6,057,124 , GRCh37.p13 chrX: 5,973,591-5,975,165 NLGN4X
    nsv7070124copy number variation1nstd229human GRCh38 chrX: 5,957,124-5,957,166 , GRCh37.p13 chrX: 5,875,165-5,875,207 NLGN4X
    nsv7069750copy number variation1nstd229human GRCh38 chrX: 5,966,643-5,966,700 , GRCh37.p13 chrX: 5,884,684-5,884,741 NLGN4X
    nsv7068708copy number variation1nstd229human GRCh38 chrX: 6,201,844-6,210,722 , GRCh37.p13 chrX: 6,119,885-6,128,763 NLGN4X
    nsv7067864copy number variation1nstd229human GRCh38 chrX: 6,123,988-6,137,388 , GRCh37.p13 chrX: 6,042,029-6,055,429 NLGN4X
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