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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148098copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427 BCL7A, HPD, 14 more genes
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv7064446inversion1nstd229human GRCh38 chr12: 121,612,208-121,754,671 , GRCh37.p13 chr12: 122,096,825-122,192,577 LOC105370034, TMEM120B, 2 more genes
    nsv6937130copy number variation1nstd229human GRCh38 chr12: 121,659,601-121,667,700 , GRCh37.p13 chr12: 122,097,507-122,105,606 MORN3, LOC105370034
    nsv6936478copy number variation1nstd229human GRCh38 chr12: 121,665,262-121,677,024 , GRCh37.p13 chr12: 122,103,168-122,114,930 MORN3, LOC105370034
    nsv6936336copy number variation1nstd229human GRCh38 chr12: 121,584,401-121,786,200 , GRCh37.p13 chr12: 122,096,825-122,224,106 RHOF, LOC105370034, 5 more genes
    nsv6935557copy number variation1nstd229human GRCh38 chr12: 121,664,167-121,785,395 , GRCh37.p13 chr12: 122,102,073-122,223,301 RHOF, MORN3, 2 more genes
    nsv6935207copy number variation1nstd229human GRCh38 chr12: 121,652,694-121,652,992 , GRCh37.p13 chr12|NW_004504303.2: 328,698-328,996 , GRCh37.p13 chr12: 122,090,600-122,090,898 MORN3
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6932943copy number variation1nstd229human GRCh38 chr12: 121,659,801-121,666,300 , GRCh37.p13 chr12: 122,097,707-122,104,206 MORN3, LOC105370034
    nsv6932022copy number variation1nstd229human GRCh38 chr12: 121,612,201-121,679,200 , GRCh37.p13 chr12: 122,050,106-122,096,824 , GRCh37.p13 chr12|NW_004504303.2: 288,204-334,922 MORN3, LOC105370034, 1 more genes
    nsv6929527copy number variation1nstd229human GRCh38 chr12: 121,630,452-121,647,322 , GRCh37.p13 chr12|NW_004504303.2: 306,456-323,326 , GRCh37.p13 chr12: 122,068,358-122,085,228 ORAI1, MORN3
    nsv6929246copy number variation1nstd229human GRCh38 chr12: 121,668,620-121,669,393 , GRCh37.p13 chr12: 122,106,526-122,107,299 MORN3, LOC105370034
    nsv6929041copy number variation1nstd229human GRCh38 chr12: 121,667,442-121,675,617 , GRCh37.p13 chr12: 122,105,348-122,113,523 MORN3, LOC105370034
    nsv6929017copy number variation1nstd229human GRCh38 chr12: 121,656,806-121,666,307 , GRCh37.p13 chr12: 122,096,825-122,104,213 MORN3, LOC105370034
    nsv6928706copy number variation1nstd229human GRCh38 chr12: 121,659,639-121,666,646 , GRCh37.p13 chr12: 122,097,545-122,104,552 MORN3, LOC105370034
    nsv6924722copy number variation1nstd229human GRCh38 chr12: 121,557,821-121,790,173 , GRCh37.p13 chr12: 122,096,825-122,228,079 KDM2B-DT, RNU6-1004P, 6 more genes
    nsv6924175copy number variation1nstd229human GRCh38 chr12: 121,643,396-121,649,811 , GRCh37.p13 chr12|NW_004504303.2: 319,400-325,815 , GRCh37.p13 chr12: 122,081,302-122,087,717 MORN3
    nsv6922937copy number variation1nstd229human GRCh38 chr12: 121,671,841-121,679,541 , GRCh37.p13 chr12: 122,109,747-122,117,447 MORN3, LOC105370034
    nsv6922829copy number variation1nstd229human GRCh38 chr12: 121,668,736-121,669,423 , GRCh37.p13 chr12: 122,106,642-122,107,329 MORN3, LOC105370034
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