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Items: 1 to 20 of 764

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146837copy number variation1nstd232human GRCh37.p13 chr22: 45,197,063-45,197,256 , GRCh38.p12 chr22: 44,801,183-44,801,376 ARHGAP8, PRR5-ARHGAP8
    nsv7098949copy number variation1nstd102humanUncertain significance GRCh38 chr22: 44,184,196-45,239,435 , GRCh37.p13 chr22: 44,580,076-45,635,316 PARVG, RTL6, 22 more genes
    nsv7074464inversion1nstd229human GRCh38 chr22: 43,918,591-49,788,574 , GRCh37.p13 chr22: 44,314,471-50,182,222 LOC107985536, LINC02939, 94 more genes
    nsv7068069inversion1nstd229human GRCh38 chr22: 44,719,122-44,872,835 , GRCh37.p13 chr22: 45,115,002-45,268,715 PRR5-ARHGAP8, LOC105373062, 2 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7061676inversion1nstd229human GRCh38 chr22: 44,757,698-44,872,616 , GRCh37.p13 chr22: 45,153,578-45,268,496 LOC105373062, ARHGAP8, 1 more genes
    nsv7037241copy number variation1nstd229human GRCh38 chr22: 44,780,544-44,872,104 , GRCh37.p13 chr22: 45,176,424-45,267,984 LOC105373062, PRR5-ARHGAP8, 1 more genes
    nsv7036792copy number variation1nstd229human GRCh38 chr22: 44,819,395-44,822,585 , GRCh37.p13 chr22: 45,215,275-45,218,465 PRR5-ARHGAP8, ARHGAP8
    nsv7036149copy number variation1nstd229human GRCh38 chr22: 44,786,169-44,786,256 , GRCh37.p13 chr22: 45,182,049-45,182,136 PRR5-ARHGAP8, ARHGAP8
    nsv7035787copy number variation1nstd229human GRCh38 chr22: 44,827,852-44,840,149 , GRCh37.p13 chr22: 45,223,732-45,236,029 ARHGAP8, PRR5-ARHGAP8
    nsv7035003copy number variation1nstd229human GRCh38 chr22: 44,819,203-44,821,948 , GRCh37.p13 chr22: 45,215,083-45,217,828 ARHGAP8, PRR5-ARHGAP8
    nsv7034536copy number variation1nstd229human GRCh38 chr22: 44,792,901-44,795,000 , GRCh37.p13 chr22: 45,188,781-45,190,880 PRR5-ARHGAP8, ARHGAP8
    nsv7034514copy number variation1nstd229human GRCh38 chr22: 44,861,260-44,879,807 , GRCh37.p13 chr22: 45,257,140-45,275,687 PRR5-ARHGAP8, ARHGAP8, 2 more genes
    nsv7034073copy number variation1nstd229human GRCh38 chr22: 44,856,563-44,857,199 , GRCh37.p13 chr22: 45,252,443-45,253,079 ARHGAP8, PRR5-ARHGAP8
    nsv7033139copy number variation1nstd229human GRCh38 chr22: 44,811,744-44,817,552 , GRCh37.p13 chr22: 45,207,624-45,213,432 PRR5-ARHGAP8, ARHGAP8
    nsv7033096copy number variation1nstd229human GRCh38 chr22: 44,719,601-44,802,200 , GRCh37.p13 chr22: 45,115,481-45,198,080 PRR5, PRR5-ARHGAP8, 1 more genes
    nsv7031630copy number variation1nstd229human GRCh38 chr22: 44,430,030-44,861,014 , GRCh37.p13 chr22: 44,825,910-45,256,894 LINC00229, LOC105373059, 11 more genes
    nsv7031135copy number variation1nstd229human GRCh38 chr22: 44,808,775-44,824,031 , GRCh37.p13 chr22: 45,204,655-45,219,911 PRR5-ARHGAP8, ARHGAP8
    nsv7030744copy number variation1nstd229human GRCh38 chr22: 44,837,306-44,840,163 , GRCh37.p13 chr22: 45,233,186-45,236,043 PRR5-ARHGAP8, ARHGAP8
    nsv7030625copy number variation1nstd229human GRCh38 chr22: 44,796,011-44,796,043 , GRCh37.p13 chr22: 45,191,891-45,191,923 ARHGAP8, PRR5-ARHGAP8
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