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Items: 1 to 20 of 1241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056109inversion1nstd229human GRCh38 chr3: 35,142,477-35,167,484 , GRCh37.p13 chr3: 35,183,969-35,208,976 LOC101928135
    nsv7051902inversion1nstd229human GRCh38 chr3: 35,083,725-35,145,917 , GRCh37.p13 chr3: 35,125,217-35,187,409 LOC101928135
    nsv7051603inversion1nstd229human GRCh38 chr3: 35,114,273-35,117,003 , GRCh37.p13 chr3: 35,155,765-35,158,495 LOC101928135
    nsv7047600inversion1nstd229human GRCh38 chr3: 35,038,142-35,141,301 , GRCh37.p13 chr3: 35,079,634-35,182,793 LOC101928135
    nsv7046251inversion1nstd229human GRCh38 chr3: 35,188,948-35,189,077 , GRCh37.p13 chr3: 35,230,440-35,230,569 LOC101928135
    nsv7045113inversion1nstd229human GRCh38 chr3: 34,864,615-34,992,246 , GRCh37.p13 chr3: 34,906,107-35,033,738 LOC101928135, FECHP1
    nsv7043704inversion1nstd229human GRCh38 chr3: 35,365,048-35,367,577 , GRCh37.p13 chr3: 35,406,540-35,409,069 LOC101928135
    nsv7042789inversion1nstd229human GRCh38 chr3: 34,079,531-36,389,791 , GRCh37.p13 chr3: 34,121,023-36,431,283 STAC, ARPP21, 9 more genes
    nsv7042277inversion1nstd229human GRCh38 chr3: 35,390,747-35,390,839 , GRCh37.p13 chr3: 35,432,239-35,432,331 LOC101928135
    nsv7041893inversion1nstd229human GRCh38 chr3: 34,995,650-34,997,838 , GRCh37.p13 chr3: 35,037,142-35,039,330 LOC101928135
    nsv6717890copy number variation1nstd229human GRCh38 chr3: 35,248,901-35,256,400 , GRCh37.p13 chr3: 35,290,393-35,297,892 RNU6-243P, LOC101928135
    nsv6717797copy number variation1nstd229human GRCh38 chr3: 35,343,664-35,358,541 , GRCh37.p13 chr3: 35,385,156-35,400,033 LOC101928135
    nsv6717497copy number variation1nstd229human GRCh38 chr3: 35,067,933-35,076,730 , GRCh37.p13 chr3: 35,109,425-35,118,222 LOC101928135
    nsv6717423copy number variation1nstd229human GRCh38 chr3: 35,150,622-35,157,038 , GRCh37.p13 chr3: 35,192,114-35,198,530 LOC101928135
    nsv6717237copy number variation1nstd229human GRCh38 chr3: 35,137,354-35,197,908 , GRCh37.p13 chr3: 35,178,846-35,239,400 LOC101928135
    nsv6716678copy number variation1nstd229human GRCh38 chr3: 35,250,407-35,252,982 , GRCh37.p13 chr3: 35,291,899-35,294,474 LOC101928135
    nsv6715776copy number variation1nstd229human GRCh38 chr3: 35,381,385-35,396,825 , GRCh37.p13 chr3: 35,422,877-35,438,317 LOC101928135
    nsv6714854copy number variation1nstd229human GRCh38 chr3: 35,272,524-35,284,179 , GRCh37.p13 chr3: 35,314,016-35,325,671 LOC101928135
    nsv6714733copy number variation1nstd229human GRCh38 chr3: 35,207,301-35,393,200 , GRCh37.p13 chr3: 35,248,793-35,434,692 RNU6-243P, LOC101928135, 1 more genes
    nsv6714593copy number variation1nstd229human GRCh38 chr3: 35,300,901-35,335,600 , GRCh37.p13 chr3: 35,342,393-35,377,092 LOC101928135
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