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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6936439copy number variation1nstd229human GRCh38 chr12: 48,909,035-48,913,947 , GRCh37.p13 chr12: 49,302,818-49,307,730 CCDC65
    nsv6925537copy number variation1nstd229human GRCh38 chr12: 48,907,346-48,912,153 , GRCh37.p13 chr12: 49,301,129-49,305,936 CCDC65
    nsv6581527inversion1nstd223human GRCh38 chr12: 48,912,148-48,913,622 , GRCh37.p13 chr12: 49,305,931-49,307,405 CCDC65
    nsv6468809copy number variation1nstd223human GRCh38 chr12: 48,901,842-48,909,259 , GRCh37.p13 chr12: 49,295,625-49,303,042 RPL32P27, CCDC65
    nsv6462754copy number variation1nstd223human GRCh38 chr12: 48,906,889-48,914,427 , GRCh37.p13 chr12: 49,300,672-49,308,210 CCDC65
    nsv6458409copy number variation1nstd223human GRCh38 chr12: 48,919,052-48,941,049 , GRCh37.p13 chr12: 49,312,835-49,334,832 CCDC65, FKBP11, 1 more genes
    nsv6273515copy number variation1nstd214human GRCh38 chr12: 48,913,124-48,913,188 , GRCh37.p13 chr12: 49,306,907-49,306,971 CCDC65
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132595copy number variation1nstd213human GRCh37 chr12: 49,290,000-49,380,001 , GRCh38.p12 chr12: 48,896,217-48,986,218 ARF3, WNT1, 7 more genes
    nsv6094652insertion1nstd212human GRCh38 chr12: 48,915,319-48,915,319 , GRCh37.p13 chr12: 49,309,102-49,309,102 CCDC65
    nsv6032747copy number variation1nstd212human GRCh38 chr12: 48,915,903-48,916,061 , GRCh37.p13 chr12: 49,309,686-49,309,844 CCDC65
    nsv6031359copy number variation1nstd212human GRCh38 chr12: 48,913,032-48,913,088 , GRCh37.p13 chr12: 49,306,815-49,306,871 CCDC65
    nsv5979692insertion1nstd209human GRCh38 chr12: 48,912,437-48,912,437 , GRCh37.p13 chr12: 49,306,220-49,306,220 CCDC65
    nsv5865919copy number variation1nstd209human GRCh38 chr12: 48,909,773-48,914,572 , GRCh37.p13 chr12: 49,303,556-49,308,355 CCDC65
    nsv5848977copy number variation1nstd209human GRCh38 chr12: 48,909,073-48,911,372 , GRCh37.p13 chr12: 49,302,856-49,305,155 CCDC65
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5512816copy number variation1nstd206human GRCh38 chr12: 48,908,387-48,909,139 , GRCh37.p13 chr12: 49,302,170-49,302,922 CCDC65
    nsv5123470mobile element insertion1nstd203human GRCh38 chr12: 48,912,437-48,912,455 , GRCh37.p13 chr12: 49,306,220-49,306,238 CCDC65
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985563copy number variation1nstd200human GRCh38 chr12: 48,919,052-48,941,049 , GRCh37.p13 chr12: 49,312,835-49,334,832 ARF3, FKBP11, 1 more genes
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