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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148136copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125 SNORD113-5, SNORD114-27, 99 more genes
    nsv7069088inversion1nstd229human GRCh38 chr14: 100,265,003-100,327,843 , GRCh37.p13 chr14: 100,731,340-100,794,180 SLC25A29, MIR6764, 4 more genes
    nsv6977301copy number variation1nstd229human GRCh38 chr14: 100,227,304-100,238,685 , GRCh37.p13 chr14: 100,693,641-100,705,022 YY1
    nsv6975895copy number variation1nstd229human GRCh38 chr14: 100,249,375-100,253,489 , GRCh37.p13 chr14: 100,715,712-100,719,826 YY1
    nsv6973543copy number variation1nstd229human GRCh38 chr14: 100,268,597-100,271,583 , GRCh37.p13 chr14: 100,734,934-100,737,920 YY1
    nsv6972696copy number variation1nstd229human GRCh38 chr14: 100,108,401-100,238,600 , GRCh37.p13 chr14: 100,574,738-100,704,937 YY1, DEGS2, 3 more genes
    nsv6972511copy number variation1nstd229human GRCh38 chr14: 100,281,701-100,287,600 , GRCh37.p13 chr14: 100,748,038-100,753,937 YY1, SLC25A29
    nsv6970765copy number variation1nstd229human GRCh38 chr14: 100,257,116-100,261,346 , GRCh37.p13 chr14: 100,723,453-100,727,683 YY1
    nsv6968325copy number variation1nstd229human GRCh38 chr14: 100,259,088-100,259,236 , GRCh37.p13 chr14: 100,725,425-100,725,573 YY1
    nsv6966575copy number variation1nstd229human GRCh38 chr14: 100,250,264-100,256,081 , GRCh37.p13 chr14: 100,716,601-100,722,418 YY1
    nsv6966034copy number variation1nstd229human GRCh38 chr14: 100,117,901-100,472,900 , GRCh37.p13 chr14: 100,584,238-100,939,237 SLC25A47, MIR345, 10 more genes
    nsv6964556copy number variation1nstd229human GRCh38 chr14: 100,278,056-100,446,082 , GRCh37.p13 chr14: 100,744,393-100,912,419 WDR25, WARS1, 7 more genes
    nsv6964374copy number variation1nstd229human GRCh38 chr14: 100,265,399-100,265,946 , GRCh37.p13 chr14: 100,731,736-100,732,283 YY1
    nsv6960942copy number variation1nstd229human GRCh38 chr14: 100,267,988-100,268,163 , GRCh37.p13 chr14: 100,734,325-100,734,500 YY1
    nsv6959430copy number variation1nstd229human GRCh38 chr14: 100,270,888-100,273,285 , GRCh37.p13 chr14: 100,737,225-100,739,622 YY1
    nsv6958941copy number variation1nstd229human GRCh38 chr14: 100,265,001-100,314,100 , GRCh37.p13 chr14: 100,731,338-100,780,437 YY1, MIR345, 2 more genes
    nsv6958655copy number variation1nstd229human GRCh38 chr14: 100,188,647-100,275,668 , GRCh37.p13 chr14: 100,654,984-100,742,005 MIR6764, YY1
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6506249copy number variation1nstd223human GRCh38 chr14: 100,257,557-100,257,634 , GRCh37.p13 chr14: 100,723,894-100,723,971 YY1
    nsv6503465copy number variation1nstd223human GRCh38 chr14: 100,273,216-100,273,616 , GRCh37.p13 chr14: 100,739,553-100,739,953 YY1
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