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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5898841copy number variation1nstd209human GRCh38 chr3: 133,485,904-133,486,226 , GRCh37.p13 chr3: 133,204,748-133,205,070 BFSP2-AS1
    nsv5893947copy number variation1nstd209human GRCh38 chr3: 133,446,570-133,446,627 , GRCh37.p13 chr3: 133,165,414-133,165,471 BFSP2-AS1, BFSP2
    nsv5610570insertion1nstd207human GRCh38 chr3: 133,425,980-133,425,980 , GRCh37.p13 chr3: 133,144,824-133,144,824 BFSP2-AS1, BFSP2
    nsv5608853insertion1nstd207human GRCh38 chr3: 133,425,964-133,425,964 , GRCh37.p13 chr3: 133,144,808-133,144,808 BFSP2-AS1, BFSP2
    nsv5606796insertion1nstd207human GRCh38 chr3: 133,425,943-133,425,943 , GRCh37.p13 chr3: 133,144,787-133,144,787 BFSP2, BFSP2-AS1
    nsv5575911copy number variation1nstd207human GRCh38 chr3: 133,485,904-133,486,226 , GRCh37.p13 chr3: 133,204,748-133,205,070 BFSP2-AS1
    nsv5570790copy number variation1nstd207human GRCh38 chr3: 133,446,570-133,446,627 , GRCh37.p13 chr3: 133,165,414-133,165,471 BFSP2, BFSP2-AS1
    nsv5543641insertion1nstd206human GRCh38 chr3: 133,482,532-133,482,582 , GRCh37.p13 chr3: 133,201,376-133,201,426 BFSP2-AS1
    nsv5453818copy number variation1nstd206human GRCh38 chr3: 133,444,798-133,444,885 , GRCh37.p13 chr3: 133,163,642-133,163,729 BFSP2-AS1, BFSP2
    nsv5452730copy number variation1nstd206human GRCh38 chr3: 133,474,508-133,474,756 , GRCh37.p13 chr3: 133,193,352-133,193,600 BFSP2-AS1, BFSP2
    nsv5450467copy number variation1nstd206human GRCh38 chr3: 133,480,395-133,495,864 , GRCh37.p13 chr3: 133,199,239-133,214,708 BFSP2-AS1, MAF1P1
    nsv5437171copy number variation1nstd206human GRCh38 chr3: 133,429,574-133,437,574 , GRCh37.p13 chr3: 133,148,418-133,156,418 BFSP2-AS1, BFSP2
    nsv5383903mobile element deletion2nstd186human GRCh37 chr3: 133,204,762-133,205,071 , GRCh38.p12 chr3: 133,485,918-133,486,227 BFSP2-AS1
    nsv5377575translocation1nstd200human GRCh38 chr3: 133,480,395-133,480,395 , GRCh38 chr3: 133,495,864-133,495,864 , GRCh37.p13 chr3: 133,199,239-133,199,239 , GRCh37.p13 chr3: 133,214,708-133,214,708 BFSP2-AS1
    nsv5351962translocation1nstd200human GRCh38 chr3: 133,490,066-133,490,066 , GRCh38 chr3: 133,490,131-133,490,131 , GRCh37.p13 chr3: 133,208,975-133,208,975 , GRCh37.p13 chr3: 133,208,910-133,208,910 BFSP2-AS1, MAF1P1
    nsv5315711copy number variation1nstd204human GRCh38.p13 chr3: 133,344,560-133,483,937 , GRCh37.p13 chr3: 133,063,404-133,202,781 BFSP2-AS1, TMEM108, 2 more genes
    nsv5227635copy number variation1nstd204human GRCh38.p13 chr3: 133,344,501-133,483,100 , GRCh37.p13 chr3: 133,063,345-133,201,944 BFSP2-AS1, LOC101927432, 2 more genes
    nsv5211231mobile element deletion1nstd204human GRCh38.p13 chr3: 133,485,916-133,486,228 , GRCh37.p13 chr3: 133,204,760-133,205,072 BFSP2-AS1
    nsv5097352mobile element insertion1nstd203human GRCh38 chr3: 133,447,894-133,447,908 , GRCh37.p13 chr3: 133,166,738-133,166,752 BFSP2, BFSP2-AS1
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