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Items: 1 to 20 of 667

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7068143inversion1nstd229human GRCh38 chr12: 19,483,414-19,490,704 , GRCh37.p13 chr12: 19,636,348-19,643,638 AEBP2
    nsv6937696copy number variation1nstd229human GRCh38 chr12: 19,471,064-19,471,185 , GRCh37.p13 chr12: 19,623,998-19,624,119 AEBP2
    nsv6937177copy number variation1nstd229human GRCh38 chr12: 19,407,172-19,438,278 , GRCh37.p13 chr12: 19,560,106-19,591,212 PDCD5P1, AEBP2
    nsv6935874copy number variation1nstd229human GRCh38 chr12: 19,320,601-19,440,100 , GRCh37.p13 chr12: 19,473,535-19,593,034 PDCD5P1, PLEKHA5, 1 more genes
    nsv6933392copy number variation1nstd229human GRCh38 chr12: 19,309,273-19,434,422 , GRCh37.p13 chr12: 19,462,207-19,587,356 PLEKHA5, AEBP2, 1 more genes
    nsv6931462copy number variation1nstd229human GRCh38 chr12: 19,400,759-19,412,535 , GRCh37.p13 chr12: 19,553,693-19,565,469 PDCD5P1, AEBP2
    nsv6929695copy number variation1nstd229human GRCh38 chr12: 19,487,126-19,493,512 , GRCh37.p13 chr12: 19,640,060-19,646,446 AEBP2
    nsv6928097copy number variation1nstd229human GRCh38 chr12: 19,212,411-19,427,488 , GRCh37.p13 chr12: 19,365,345-19,580,422 PLEKHA5, PDCD5P1, 3 more genes
    nsv6925710copy number variation1nstd229human GRCh38 chr12: 19,331,201-19,518,000 , GRCh37.p13 chr12: 19,484,135-19,670,934 AEBP2, PLEKHA5, 4 more genes
    nsv6923784copy number variation1nstd229human GRCh38 chr12: 19,468,480-19,479,653 , GRCh37.p13 chr12: 19,621,414-19,632,587 AEBP2
    nsv6922138copy number variation1nstd229human GRCh38 chr12: 19,520,927-19,524,262 , GRCh37.p13 chr12: 19,673,861-19,677,196 AEBP2
    nsv6921660copy number variation1nstd229human GRCh38 chr12: 19,433,119-19,433,430 , GRCh37.p13 chr12: 19,586,053-19,586,364 AEBP2
    nsv6921598copy number variation1nstd229human GRCh38 chr12: 19,434,210-19,434,266 , GRCh37.p13 chr12: 19,587,144-19,587,200 AEBP2
    nsv6921437copy number variation1nstd229human GRCh38 chr12: 19,422,323-19,426,390 , GRCh37.p13 chr12: 19,575,257-19,579,324 AEBP2
    nsv6920940copy number variation1nstd229human GRCh38 chr12: 19,320,901-19,469,300 , GRCh37.p13 chr12: 19,473,835-19,622,234 PLEKHA5, AEBP2, 3 more genes
    nsv6920196copy number variation1nstd229human GRCh38 chr12: 19,412,703-19,417,972 , GRCh37.p13 chr12: 19,565,637-19,570,906 PDCD5P1, AEBP2
    nsv6919880copy number variation1nstd229human GRCh38 chr12: 19,315,108-19,427,542 , GRCh37.p13 chr12: 19,468,042-19,580,476 PDCD5P1, PLEKHA5, 1 more genes
    nsv6919763copy number variation1nstd229human GRCh38 chr12: 19,463,896-19,466,022 , GRCh37.p13 chr12: 19,616,830-19,618,956 AEBP2
    nsv6635227copy number variation1nstd227human GRCh38.p12 chr12: 19,301,473-19,410,019 , GRCh37 chr12: 19,454,407-19,562,953 PLEKHA5, AEBP2, 2 more genes
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