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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6717272copy number variation1nstd229human GRCh38 chr3: 48,371,817-48,372,028 , GRCh37.p13 chr3: 48,413,307-48,413,518 FBXW12
    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
    nsv6705885copy number variation1nstd229human GRCh38 chr3: 48,381,201-48,393,000 , GRCh37.p13 chr3: 48,422,691-48,434,464 FBXW12
    nsv6703711copy number variation1nstd229human GRCh38 chr3: 48,394,059-48,397,222 , GRCh37.p13 chr3: 48,435,524-48,438,688 FBXW12
    nsv6703359copy number variation1nstd229human GRCh38 chr3: 48,387,260-48,392,862 , GRCh37.p13 chr3: 48,428,751-48,434,337 FBXW12
    nsv6703202copy number variation1nstd229human GRCh38 chr3: 48,367,801-48,375,300 , GRCh37.p13 chr3: 48,409,291-48,416,790 FBXW12
    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
    nsv6700694copy number variation1nstd229human GRCh38 chr3: 48,393,258-48,408,532 , GRCh37.p13 chr3: 48,434,722-48,449,939 FBXW12, PLXNB1
    nsv6699993copy number variation1nstd229human GRCh38 chr3: 48,210,301-48,393,400 , GRCh37.p13 chr3: 48,251,791-48,434,864 ZNF589, FCF1P2, 7 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
    nsv6543522inversion1nstd223human GRCh38 chr3: 48,392,453-48,392,788 , GRCh37.p13 chr3: 48,433,929-48,434,263 FBXW12
    nsv6374723copy number variation1nstd223human GRCh38 chr3: 48,388,690-48,395,287 , GRCh37.p13 chr3: 48,430,178-48,436,752 FBXW12
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6368296copy number variation1nstd223human GRCh38 chr3: 48,370,501-48,380,200 , GRCh37.p13 chr3: 48,411,991-48,421,690 FBXW12, RN7SL321P
    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
    nsv6253984mobile element insertion1nstd215human GRCh38 chr3: 48,387,259-48,387,259 , GRCh37.p13 chr3: 48,428,750-48,428,750 FBXW12
    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
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5452640copy number variation1nstd206human GRCh38 chr3: 48,381,286-48,382,353 , GRCh37.p13 chr3: 48,422,776-48,423,843 FBXW12
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