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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146877copy number variation1nstd232human GRCh37.p13 chr2: 143,927,272-143,927,331 , GRCh38.p12 chr2: 143,169,703-143,169,762 ARHGAP15, LOC107985949
    nsv7054361inversion1nstd229human GRCh38 chr2: 143,314,758-143,316,598 , GRCh37.p13 chr2: 144,072,327-144,074,167 ARHGAP15
    nsv7051918inversion1nstd229human GRCh38 chr2: 143,360,660-143,364,177 , GRCh37.p13 chr2: 144,118,229-144,121,746 ARHGAP15
    nsv7049242inversion1nstd229human GRCh38 chr2: 141,675,999-143,767,674 , GRCh37.p13 chr2: 142,433,568-144,525,243 MTND3P9, LOC101928361, 20 more genes
    nsv7046162inversion1nstd229human GRCh38 chr2: 143,317,186-143,317,220 , GRCh37.p13 chr2: 144,074,755-144,074,789 ARHGAP15
    nsv7041292inversion1nstd229human GRCh38 chr2: 143,261,141-143,261,193 , GRCh37.p13 chr2: 144,018,710-144,018,762 ARHGAP15
    nsv6697581copy number variation1nstd229human GRCh38 chr2: 143,526,104-143,526,436 , GRCh37.p13 chr2: 144,283,673-144,284,005 ARHGAP15
    nsv6697552copy number variation1nstd229human GRCh38 chr2: 143,363,275-143,375,066 , GRCh37.p13 chr2: 144,120,844-144,132,635 ARHGAP15
    nsv6697278copy number variation1nstd229human GRCh38 chr2: 143,406,601-143,412,200 , GRCh37.p13 chr2: 144,164,170-144,169,769 ARHGAP15
    nsv6697079copy number variation1nstd229human GRCh38 chr2: 143,579,401-143,583,100 , GRCh37.p13 chr2: 144,336,970-144,340,669 ARHGAP15
    nsv6695961copy number variation1nstd229human GRCh38 chr2: 143,421,586-143,424,460 , GRCh37.p13 chr2: 144,179,155-144,182,029 ARHGAP15
    nsv6695669copy number variation1nstd229human GRCh38 chr2: 143,291,421-143,291,508 , GRCh37.p13 chr2: 144,048,990-144,049,077 ARHGAP15
    nsv6695576copy number variation1nstd229human GRCh38 chr2: 143,131,641-143,135,046 , GRCh37.p13 chr2: 143,889,210-143,892,615 ARHGAP15
    nsv6695532copy number variation1nstd229human GRCh38 chr2: 143,721,400-143,725,304 , GRCh37.p13 chr2: 144,478,969-144,482,873 ARHGAP15, ARHGAP15-AS1
    nsv6695380copy number variation1nstd229human GRCh38 chr2: 143,427,301-143,430,600 , GRCh37.p13 chr2: 144,184,870-144,188,169 ARHGAP15
    nsv6695287copy number variation1nstd229human GRCh38 chr2: 143,123,066-143,129,108 , GRCh37.p13 chr2: 143,880,635-143,886,677 ARHGAP15
    nsv6694860copy number variation1nstd229human GRCh38 chr2: 143,452,472-143,462,618 , GRCh37.p13 chr2: 144,210,041-144,220,187 ARHGAP15
    nsv6694576copy number variation1nstd229human GRCh38 chr2: 143,471,187-143,471,232 , GRCh37.p13 chr2: 144,228,756-144,228,801 ARHGAP15
    nsv6693942copy number variation1nstd229human GRCh38 chr2: 143,632,274-143,650,376 , GRCh37.p13 chr2: 144,389,843-144,407,945 ARHGAP15, ARHGAP15-AS1
    nsv6693540copy number variation1nstd229human GRCh38 chr2: 143,329,441-143,590,258 , GRCh37.p13 chr2: 144,087,010-144,347,827 ARHGAP15
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