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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147747insertion1nstd232human GRCh37.p13 chr3: 33,870,461-33,870,461 , GRCh38.p12 chr3: 33,828,969-33,828,969 PDCD6IP
    nsv7144484insertion1nstd232human GRCh37.p13 chr3: 33,840,429-33,840,429 , GRCh38.p12 chr3: 33,798,937-33,798,937 PDCD6IP, PDCD6IP-DT
    nsv6714375copy number variation1nstd229human GRCh38 chr3: 33,854,776-34,159,221 , GRCh37.p13 chr3: 33,896,268-34,200,713 LOC105377024, PDCD6IP, 1 more genes
    nsv6712380copy number variation1nstd229human GRCh38 chr3: 33,837,972-33,838,052 , GRCh37.p13 chr3: 33,879,464-33,879,544 PDCD6IP
    nsv6709671copy number variation1nstd229human GRCh38 chr3: 33,814,589-38,161,211 , GRCh37.p13 chr3: 33,856,081-38,202,702 RFC3P1, ITGA9, 51 more genes
    nsv6709229copy number variation1nstd229human GRCh38 chr3: 33,814,401-33,815,400 , GRCh37.p13 chr3: 33,855,893-33,856,892 PDCD6IP
    nsv6704503copy number variation1nstd229human GRCh38 chr3: 33,759,801-33,824,600 , GRCh37.p13 chr3: 33,801,293-33,866,092 PDCD6IP, SDAD1P3, 1 more genes
    nsv6701216copy number variation1nstd229human GRCh38 chr3: 33,870,109-33,870,249 , GRCh37.p13 chr3: 33,911,601-33,911,741 PDCD6IP
    nsv6539643inversion1nstd223human GRCh38 chr3: 33,823,642-33,824,555 , GRCh37.p13 chr3: 33,865,134-33,866,047 PDCD6IP
    nsv6370115copy number variation1nstd223human GRCh38 chr3: 33,831,049-33,831,761 , GRCh37.p13 chr3: 33,872,541-33,873,253 PDCD6IP
    nsv6313757copy number variation1nstd102humanUncertain significance GRCh37 chr3: 32,699,328-35,286,114 , GRCh38.p12 chr3: 32,657,836-35,244,622 CRTAP, FECHP1, 26 more genes
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6299892copy number variation1nstd186human GRCh37 chr3: 33,902,208-33,902,261 , GRCh38.p12 chr3: 33,860,716-33,860,769 PDCD6IP
    nsv6279990insertion1nstd214human GRCh38 chr3: 33,818,850-33,818,850 , GRCh37.p13 chr3: 33,860,342-33,860,342 PDCD6IP
    nsv6148545copy number variation1nstd214human GRCh38 chr3: 33,837,972-33,838,051 , GRCh37.p13 chr3: 33,879,464-33,879,543 PDCD6IP
    nsv5993107copy number variation1nstd212human GRCh38 chr3: 33,800,477-33,800,537 , GRCh37.p13 chr3: 33,841,969-33,842,029 PDCD6IP
    nsv5889018copy number variation1nstd209human GRCh38 chr3: 33,837,972-33,838,051 , GRCh37.p13 chr3: 33,879,464-33,879,543 PDCD6IP
    nsv5688100mobile element insertion1nstd211human GRCh38 chr3: 33,812,702-33,812,702 , GRCh37.p13 chr3: 33,854,194-33,854,194 PDCD6IP
    nsv5678865mobile element insertion2nstd211human GRCh38 chr3: 33,847,407-33,847,407 , GRCh37.p13 chr3: 33,888,899-33,888,899 PDCD6IP
    nsv5443768copy number variation1nstd206human GRCh38 chr3: 33,806,121-33,806,298 , GRCh37.p13 chr3: 33,847,613-33,847,790 PDCD6IP
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