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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6856315copy number variation1nstd229human GRCh38 chr8: 69,716,010-70,222,698 , GRCh37.p13 chr8: 70,628,245-71,134,933 RN7SL675P, RNA5SP270, 10 more genes
    nsv6847500copy number variation1nstd229human GRCh38 chr8: 69,981,001-70,076,300 , GRCh37.p13 chr8: 70,893,236-70,988,535 RNU1-101P, SUMO2P20, 1 more genes
    nsv6847116copy number variation1nstd229human GRCh38 chr8: 68,675,587-70,209,684 , GRCh37.p13 chr8: 69,587,822-71,121,919 LINC01603, SUMO2P20, 20 more genes
    nsv6843492copy number variation1nstd229human GRCh38 chr8: 69,973,168-70,079,148 , GRCh37.p13 chr8: 70,885,403-70,991,383 SUMO2P20, RNU1-101P, 1 more genes
    nsv6841945copy number variation1nstd229human GRCh38 chr8: 70,056,764-70,062,759 , GRCh37.p13 chr8: 70,968,999-70,974,994 PRDM14
    nsv6841175copy number variation1nstd229human GRCh38 chr8: 69,156,248-70,149,472 , GRCh37.p13 chr8: 70,068,483-71,061,707 RN7SL675P, H2AZP2, 14 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6633104copy number variation1nstd224human GRCh37 chr8: 70,854,206-70,981,780 , GRCh38.p12 chr8: 69,941,971-70,069,545 SDCBPP2, SUMO2P20, 1 more genes
    nsv6568976inversion1nstd223human GRCh38 chr8: 70,059,115-70,059,924 , GRCh37.p13 chr8: 70,971,350-70,972,159 PRDM14
    nsv6568553inversion1nstd223human GRCh38 chr8: 69,899,793-71,797,262 , GRCh37.p13 chr8: 70,812,028-72,709,497 EYA1, SDCBPP2, 24 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6304829copy number variation1nstd186human GRCh37 chr8: 70,976,980-70,977,341 , GRCh38.p12 chr8: 70,064,745-70,065,106 PRDM14
    nsv6291265copy number variation1nstd102humanPathogenic GRCh37 chr8: 69,894,553-72,597,645 , GRCh38.p12 chr8: 68,982,318-71,685,410 LINC01603, LINC03020, 34 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136594copy number variation1nstd213human GRCh37 chr8: 70,060,000-72,060,001 , GRCh38.p12 chr8: 69,147,765-71,147,766 NCOA2, TRAM1, 26 more genes
    nsv6005913copy number variation1nstd212human GRCh38 chr8: 70,063,235-70,063,366 , GRCh37.p13 chr8: 70,975,470-70,975,601 PRDM14
    nsv5974932inversion1nstd209human GRCh38 chr8: 70,050,413-70,058,706 , GRCh37.p13 chr8: 70,962,648-70,970,941 PRDM14
    nsv5854773copy number variation1nstd209human GRCh38 chr8: 70,048,842-70,050,441 , GRCh37.p13 chr8: 70,961,077-70,962,676 PRDM14
    nsv5483115copy number variation1nstd206human GRCh38 chr8: 69,999,352-70,051,284 , GRCh37.p13 chr8: 70,911,587-70,963,519 PRDM14
    nsv5479878copy number variation1nstd206human GRCh38 chr8: 70,064,745-70,065,106 , GRCh37.p13 chr8: 70,976,980-70,977,341 PRDM14
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