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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098697insertion3nstd102humanPathogenic GRCh38 chr4: 41,745,972-41,746,045 , GRCh37.p13 chr4: 41,747,989-41,748,062 PHOX2B
    nsv6634498copy number variation1nstd102humanUncertain significance GRCh38 chr4: 41,745,946-41,746,014 , GRCh37 chr4: 41,747,963-41,748,031 PHOX2B
    nsv6729051copy number variation1nstd229human GRCh38 chr4: 41,818,629-41,832,220 , GRCh37.p13 chr4: 41,820,646-41,834,237 PHOX2B-AS1
    nsv6726861copy number variation1nstd229human GRCh38 chr4: 41,807,970-41,814,209 , GRCh37.p13 chr4: 41,809,987-41,816,226 PHOX2B-AS1
    nsv6728179copy number variation1nstd229human GRCh38 chr4: 41,738,290-41,742,669 , GRCh37.p13 chr4: 41,740,307-41,744,686 PHOX2B
    nsv6734071copy number variation1nstd229human GRCh38 chr4: 41,800,662-41,804,292 , GRCh37.p13 chr4: 41,802,679-41,806,309 PHOX2B-AS1
    nsv6724180copy number variation1nstd229human GRCh38 chr4: 41,811,338-41,814,488 , GRCh37.p13 chr4: 41,813,355-41,816,505 PHOX2B-AS1
    nsv6727332copy number variation1nstd229human GRCh38 chr4: 41,850,888-41,853,695 , GRCh37.p13 chr4: 41,852,905-41,855,712 PHOX2B-AS1
    nsv6732597copy number variation1nstd229human GRCh38 chr4: 41,776,162-41,778,211 , GRCh37.p13 chr4: 41,778,179-41,780,228 PHOX2B-AS1
    nsv6725552copy number variation1nstd229human GRCh38 chr4: 41,803,551-41,803,588 , GRCh37.p13 chr4: 41,805,568-41,805,605 PHOX2B-AS1
    nsv6385611copy number variation1nstd223human GRCh38 chr4: 41,798,332-41,812,180 , GRCh37.p13 chr4: 41,800,349-41,814,197 PHOX2B-AS1
    nsv6381586copy number variation1nstd223human GRCh38 chr4: 41,849,024-41,853,637 , GRCh37.p13 chr4: 41,851,041-41,855,654 PHOX2B-AS1
    nsv6389640copy number variation1nstd223human GRCh38 chr4: 41,800,662-41,804,289 , GRCh37.p13 chr4: 41,802,679-41,806,306 PHOX2B-AS1
    nsv6376319copy number variation1nstd223human GRCh38 chr4: 41,853,994-41,854,611 , GRCh37.p13 chr4: 41,856,011-41,856,628 PHOX2B-AS1
    nsv6393454copy number variation1nstd223human GRCh38 chr4: 41,830,168-41,830,643 , GRCh37.p13 chr4: 41,832,185-41,832,660 PHOX2B-AS1
    nsv6393790copy number variation1nstd223human GRCh38 chr4: 41,809,877-41,810,192 , GRCh37.p13 chr4: 41,811,894-41,812,209 PHOX2B-AS1
    nsv6379730copy number variation1nstd223human GRCh38 chr4: 41,791,453-41,791,722 , GRCh37.p13 chr4: 41,793,470-41,793,739 PHOX2B-AS1
    nsv6390022copy number variation1nstd223human GRCh38 chr4: 41,804,274-41,804,529 , GRCh37.p13 chr4: 41,806,291-41,806,546 PHOX2B-AS1
    nsv5460493copy number variation1nstd206human GRCh38 chr4: 41,804,277-41,804,529 , GRCh37.p13 chr4: 41,806,294-41,806,546 PHOX2B-AS1
    nsv5997308copy number variation1nstd212human GRCh38 chr4: 41,849,044-41,849,105 , GRCh37.p13 chr4: 41,851,061-41,851,122 PHOX2B-AS1
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