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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095783copy number variation1nstd102humanUncertain significance GRCh37 chr1: 213,224,747-213,224,871 , GRCh38.p12 chr1: 213,051,405-213,051,529 RPS6KC1
    nsv7057362inversion1nstd229human GRCh38 chr1: 213,205,948-213,521,862 , GRCh37.p13 chr1: 213,379,291-213,695,205 RPL31P13, RPS6KC1
    nsv7053438inversion1nstd229human GRCh38 chr1: 213,160,412-213,162,483 , GRCh37.p13 chr1: 213,333,755-213,335,826 RPS6KC1
    nsv7041947inversion1nstd229human GRCh38 chr1: 213,058,876-213,063,521 , GRCh37.p13 chr1: 213,232,218-213,236,863 RPS6KC1
    nsv6675737copy number variation1nstd229human GRCh38 chr1: 213,137,401-213,146,800 , GRCh37.p13 chr1: 213,310,744-213,320,143 RPS6KC1
    nsv6675223copy number variation1nstd229human GRCh38 chr1: 213,213,801-213,221,600 , GRCh37.p13 chr1: 213,387,144-213,394,943 RPS6KC1
    nsv6674386copy number variation1nstd229human GRCh38 chr1: 213,189,201-213,202,700 , GRCh37.p13 chr1: 213,362,544-213,376,043 RPS6KC1
    nsv6673697copy number variation1nstd229human GRCh38 chr1: 213,049,495-213,228,388 , GRCh37.p13 chr1: 213,222,837-213,401,731 RPS6KC1
    nsv6673205copy number variation1nstd229human GRCh38 chr1: 213,139,102-213,146,881 , GRCh37.p13 chr1: 213,312,445-213,320,224 RPS6KC1
    nsv6672064copy number variation1nstd229human GRCh38 chr1: 213,281,006-213,283,561 , GRCh37.p13 chr1: 213,454,349-213,456,904 RPS6KC1
    nsv6671808copy number variation1nstd229human GRCh38 chr1: 213,266,401-213,268,400 , GRCh37.p13 chr1: 213,439,744-213,441,743 RPS6KC1
    nsv6671672copy number variation1nstd229human GRCh38 chr1: 212,832,753-213,257,197 , GRCh37.p13 chr1: 213,006,095-213,430,540 RPS28P2, RPS6KC1, 5 more genes
    nsv6671175copy number variation1nstd229human GRCh38 chr1: 213,216,901-213,217,300 , GRCh37.p13 chr1: 213,390,244-213,390,643 RPS6KC1
    nsv6670855copy number variation1nstd229human GRCh38 chr1: 213,359,960-213,363,228 , GRCh37.p13 chr1: 213,533,303-213,536,571 RPS6KC1
    nsv6669976copy number variation1nstd229human GRCh38 chr1: 213,156,801-213,158,700 , GRCh37.p13 chr1: 213,330,144-213,332,043 RPS6KC1
    nsv6669140copy number variation1nstd229human GRCh38 chr1: 213,200,174-213,205,152 , GRCh37.p13 chr1: 213,373,517-213,378,495 RPS6KC1
    nsv6668815copy number variation1nstd229human GRCh38 chr1: 213,187,690-213,200,659 , GRCh37.p13 chr1: 213,361,033-213,374,002 RPS6KC1
    nsv6665349copy number variation1nstd229human GRCh38 chr1: 213,141,801-213,146,900 , GRCh37.p13 chr1: 213,315,144-213,320,243 RPS6KC1
    nsv6665251copy number variation1nstd229human GRCh38 chr1: 213,370,120-213,372,379 , GRCh37.p13 chr1: 213,543,463-213,545,722 RPS6KC1
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