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Items: 1 to 20 of 769

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137756copy number variation1nstd232human GRCh37.p13 chr9: 35,183,031-35,183,104 , GRCh38.p12 chr9: 35,183,034-35,183,107 UNC13B
    nsv7098455copy number variation6nstd102humanUncertain significance GRCh37 chr9: 32,453,279-37,785,041 , GRCh38.p12 chr9: 32,453,281-37,785,044 TRBVAOR9-2, UBAP2, 197 more genes
    nsv7098082copy number variation1nstd102humanUncertain significance GRCh37 chr9: 34,370,797-36,276,941 , GRCh38.p12 chr9: 34,370,799-36,276,944 UNC13B, CD72, 86 more genes
    nsv7074600inversion1nstd229human GRCh38 chr9: 35,327,318-35,329,860 , GRCh37.p13 chr9: 35,327,315-35,329,857 UNC13B
    nsv7074026inversion1nstd229human GRCh38 chr9: 35,243,924-35,243,962 , GRCh37.p13 chr9: 35,243,921-35,243,959 UNC13B
    nsv7067519inversion1nstd229human GRCh38 chr9: 35,185,927-35,186,070 , GRCh37.p13 chr9: 35,185,924-35,186,067 UNC13B
    nsv7066996inversion1nstd229human GRCh38 chr9: 35,240,127-35,414,862 , GRCh37.p13 chr9: 35,240,124-35,414,859 UNC13B, ATP8B5P
    nsv7060547inversion1nstd229human GRCh38 chr9: 35,282,974-35,527,178 , GRCh37.p13 chr9: 35,282,971-35,527,175 RUSC2, LOC105376026, 4 more genes
    nsv7060440inversion1nstd229human GRCh38 chr9: 33,533,890-38,610,880 , GRCh37.p13 chr9: 33,533,888-38,610,877 FRMPD1, PTENP1, 182 more genes
    nsv7058978inversion1nstd229human GRCh38 chr9: 33,570,636-38,550,207 , GRCh37.p13 chr9: 33,570,634-38,550,204 TRBV29OR9-2, SPMIP6, 180 more genes
    nsv6877872copy number variation1nstd229human GRCh38 chr9: 35,169,401-35,175,700 , GRCh37.p13 chr9: 35,169,398-35,175,697 UNC13B
    nsv6877586copy number variation1nstd229human GRCh38 chr9: 35,364,132-35,364,314 , GRCh37.p13 chr9: 35,364,129-35,364,311 UNC13B
    nsv6877546copy number variation1nstd229human GRCh38 chr9: 35,161,160-35,408,187 , GRCh37.p13 chr9: 35,161,157-35,408,184 UNC13B, ATP8B5P
    nsv6876941copy number variation1nstd229human GRCh38 chr9: 35,241,101-35,283,000 , GRCh37.p13 chr9: 35,241,098-35,282,997 UNC13B
    nsv6876758copy number variation1nstd229human GRCh38 chr9: 35,305,106-35,310,358 , GRCh37.p13 chr9: 35,305,103-35,310,355 UNC13B
    nsv6876510copy number variation1nstd229human GRCh38 chr9: 35,170,369-35,174,529 , GRCh37.p13 chr9: 35,170,366-35,174,526 UNC13B
    nsv6875731copy number variation1nstd229human GRCh38 chr9: 35,371,517-35,371,542 , GRCh37.p13 chr9: 35,371,514-35,371,539 UNC13B
    nsv6874811copy number variation1nstd229human GRCh38 chr9: 35,237,827-35,238,547 , GRCh37.p13 chr9: 35,237,824-35,238,544 UNC13B
    nsv6874620copy number variation1nstd229human GRCh38 chr9: 35,210,597-35,355,016 , GRCh37.p13 chr9: 35,210,594-35,355,013 UNC13B
    nsv6871800copy number variation1nstd229human GRCh38 chr9: 35,256,280-35,257,070 , GRCh37.p13 chr9: 35,256,277-35,257,067 UNC13B
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