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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
    nsv7088754copy number variation1nstd229human GRCh38 chrX: 72,229,301-72,388,400 , GRCh37.p13 chrX: 71,449,151-71,530,833 CITED1, LOC105373250, 5 more genes
    nsv7088753copy number variation1nstd229human GRCh38 chrX: 72,195,069-72,195,583 , GRCh37.p13 chrX: 71,414,919-71,415,433 PIN4
    nsv7088752copy number variation1nstd229human GRCh38 chrX: 72,194,882-72,195,339 , GRCh37.p13 chrX: 71,414,732-71,415,189 PIN4
    nsv7088751copy number variation1nstd229human GRCh38 chrX: 72,193,703-72,194,807 , GRCh37.p13 chrX: 71,413,553-71,414,657 PIN4
    nsv7088750copy number variation1nstd229human GRCh38 chrX: 72,192,701-72,194,900 , GRCh37.p13 chrX: 71,412,551-71,414,750 PIN4
    nsv7088749copy number variation1nstd229human GRCh38 chrX: 72,192,301-72,196,600 , GRCh37.p13 chrX: 71,412,151-71,416,450 PIN4
    nsv7088748copy number variation1nstd229human GRCh38 chrX: 72,190,901-72,196,400 , GRCh37.p13 chrX: 71,410,751-71,416,250 PIN4
    nsv7088747copy number variation1nstd229human GRCh38 chrX: 72,190,207-72,190,267 , GRCh37.p13 chrX: 71,410,057-71,410,117 PIN4
    nsv7088746copy number variation1nstd229human GRCh38 chrX: 72,189,738-72,190,513 , GRCh37.p13 chrX: 71,409,588-71,410,363 PIN4
    nsv7088745copy number variation1nstd229human GRCh38 chrX: 72,189,478-72,190,129 , GRCh37.p13 chrX: 71,409,328-71,409,979 PIN4
    nsv7088744copy number variation1nstd229human GRCh38 chrX: 72,189,101-72,197,700 , GRCh37.p13 chrX: 71,408,951-71,417,550 PIN4, RN7SL388P
    nsv7088743copy number variation1nstd229human GRCh38 chrX: 72,187,001-72,196,600 , GRCh37.p13 chrX: 71,406,851-71,416,450 PIN4
    nsv7088742copy number variation1nstd229human GRCh38 chrX: 72,186,201-72,196,500 , GRCh37.p13 chrX: 71,406,051-71,416,350 PIN4
    nsv7088741copy number variation1nstd229human GRCh38 chrX: 72,175,001-72,180,100 , GRCh37.p13 chrX: 71,394,851-71,399,950 PIN4
    nsv7088740copy number variation1nstd229human GRCh38 chrX: 72,170,066-72,181,107 , GRCh37.p13 chrX: 71,389,916-71,400,957 PIN4
    nsv7023554inversion1nstd229human GRCh38 chrX: 71,874,497-72,559,896 , GRCh37.p13 chrX: 71,094,347-71,530,833 NHSL2, CITED1, 10 more genes
    nsv7018592inversion1nstd229human GRCh38 chrX: 71,642,458-75,115,067 , GRCh37.p13 chrX: 70,862,308-74,334,902 RN7SL648P, LOC101059915, 83 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
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