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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147456insertion1nstd232human GRCh37.p13 chr3: 48,224,520-48,224,520 , GRCh38.p12 chr3: 48,183,030-48,183,030 CDC25A
    nsv7145795insertion1nstd232human GRCh37.p13 chr3: 48,215,947-48,215,947 , GRCh38.p12 chr3: 48,174,457-48,174,457 CDC25A
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv7047381inversion1nstd229human GRCh38 chr3: 47,589,597-48,210,528 , GRCh37.p13 chr3: 47,631,087-48,252,018 CDC25A, SNORD146, 12 more genes
    nsv6717954copy number variation1nstd229human GRCh38 chr3: 47,896,028-48,196,668 , GRCh37.p13 chr3: 47,937,518-48,238,158 MAP4, RN7SL664P, 7 more genes
    nsv6716459copy number variation1nstd229human GRCh38 chr3: 48,184,978-48,207,362 , GRCh37.p13 chr3: 48,226,468-48,248,852 MIR4443, CDC25A
    nsv6711899copy number variation1nstd229human GRCh38 chr3: 48,176,901-48,213,600 , GRCh37.p13 chr3: 48,218,391-48,255,090 CDC25A, RNU7-128P, 2 more genes
    nsv6709380copy number variation1nstd229human GRCh38 chr3: 47,729,831-48,514,976 , GRCh37.p13 chr3: 47,771,321-48,552,409 ATRIP-TREX1, PLXNB1, 26 more genes
    nsv6702121copy number variation1nstd229human GRCh38 chr3: 48,144,437-48,158,494 , GRCh37.p13 chr3: 48,185,927-48,199,984 CDC25A
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6700723copy number variation1nstd229human GRCh38 chr3: 48,186,149-48,186,292 , GRCh37.p13 chr3: 48,227,639-48,227,782 CDC25A
    nsv6700305copy number variation1nstd229human GRCh38 chr3: 47,915,855-48,166,913 , GRCh37.p13 chr3: 47,957,345-48,208,403 SNRPFP4, RPL17P16, 4 more genes
    nsv6698688copy number variation1nstd229human GRCh38 chr3: 48,100,012-48,509,466 , GRCh37.p13 chr3: 48,141,502-48,546,899 MIR4443, RNU7-128P, 20 more genes
    nsv6358697copy number variation1nstd223human GRCh38 chr3: 48,136,256-48,160,526 , GRCh37.p13 chr3: 48,177,746-48,202,016 SNRPFP4, CDC25A
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6263471copy number variation1nstd214human GRCh38 chr3: 48,155,635-48,155,766 , GRCh37.p13 chr3: 48,197,125-48,197,256 CDC25A
    nsv6253982mobile element insertion1nstd215human GRCh38 chr3: 48,156,511-48,156,511 , GRCh37.p13 chr3: 48,198,001-48,198,001 CDC25A
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5994103copy number variation1nstd212human GRCh38 chr3: 48,155,576-48,155,719 , GRCh37.p13 chr3: 48,197,066-48,197,209 CDC25A
    nsv5993486copy number variation1nstd212human GRCh38 chr3: 48,170,278-48,170,677 , GRCh37.p13 chr3: 48,211,768-48,212,167 CDC25A
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