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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6118378copy number variation1nstd186human GRCh37 chr3: 137,913,138-137,913,247 , GRCh38.p12 chr3: 138,194,296-138,194,405 ARMC8
    nsv5965806insertion1nstd209human GRCh38 chr3: 138,272,408-138,272,408 , GRCh37.p13 chr3: 137,991,250-137,991,250 NME9, ARMC8
    nsv5906122copy number variation1nstd209human GRCh38 chr3: 138,264,758-138,264,812 , GRCh37.p13 chr3: 137,983,600-137,983,654 NME9, ARMC8
    nsv5904487copy number variation1nstd209human GRCh38 chr3: 138,194,293-138,194,404 , GRCh37.p13 chr3: 137,913,135-137,913,246 ARMC8
    nsv5889866copy number variation1nstd209human GRCh38 chr3: 137,097,814-139,588,879 , GRCh37.p13 chr3: 136,816,656-139,307,721 , LOC105374127, 42 more genes
    nsv5834938copy number variation1nstd209human GRCh38 chr3: 138,220,856-138,222,634 , GRCh37.p13 chr3: 137,939,698-137,941,476 ARMC8
    nsv5692750mobile element insertion1nstd211human GRCh38 chr3: 138,296,552-138,296,552 , GRCh37.p13 chr3: 138,015,394-138,015,394 NME9, ARMC8
    nsv5687639mobile element insertion2nstd211human GRCh38 chr3: 138,272,419-138,272,419 , GRCh37.p13 chr3: 137,991,261-137,991,261 ARMC8, NME9
    nsv5676324mobile element insertion1nstd211human GRCh38 chr3: 138,243,622-138,243,622 , GRCh37.p13 chr3: 137,962,464-137,962,464 ARMC8
    nsv5582226copy number variation1nstd207human GRCh38 chr3: 138,194,293-138,194,404 , GRCh37.p13 chr3: 137,913,135-137,913,246 ARMC8
    nsv5556310sequence alteration1nstd206human GRCh38 chr3: 138,197,674-138,205,917 , GRCh37.p13 chr3: 137,916,516-137,924,759 ARMC8
    nsv5453618copy number variation1nstd206human GRCh38 chr3: 138,130,649-138,217,748 , GRCh37.p13 chr3: 137,849,491-137,936,590 ARMC8, DBR1, 1 more genes
    nsv5436421copy number variation1nstd206human GRCh38 chr3: 138,264,758-138,264,824 , GRCh37.p13 chr3: 137,983,600-137,983,666 NME9, ARMC8
    nsv5435157copy number variation1nstd206human GRCh38 chr3: 138,194,296-138,194,405 , GRCh37.p13 chr3: 137,913,138-137,913,247 ARMC8
    nsv5398422mobile element insertion1nstd206human GRCh38 chr3: 138,272,419-138,272,470 , GRCh37.p13 chr3: 137,991,261-137,991,312 ARMC8, NME9
    nsv5361942translocation1nstd200human GRCh38 chr3: 138,205,918-138,205,918 , GRCh38 chr3: 138,200,016-138,200,016 , GRCh37.p13 chr3: 137,918,858-137,918,858 , GRCh37.p13 chr3: 137,924,760-137,924,760 ARMC8
    nsv5361941translocation1nstd200human GRCh38 chr3: 138,204,286-138,204,286 , GRCh38 chr3: 138,197,674-138,197,674 , GRCh37.p13 chr3: 137,923,128-137,923,128 , GRCh37.p13 chr3: 137,916,516-137,916,516 ARMC8
    nsv5346576translocation1nstd200human GRCh38 chr3: 138,264,758-138,264,758 , GRCh38 chr3: 138,264,824-138,264,824 , GRCh37.p13 chr3: 137,983,666-137,983,666 , GRCh37.p13 chr3: 137,983,600-137,983,600 ARMC8, NME9
    nsv5344794translocation1nstd200human GRCh37 chr3: 137,924,760-137,924,760 , GRCh37 chr3: 137,918,858-137,918,858 , GRCh38.p12 chr3: 138,205,918-138,205,918 , GRCh38.p12 chr3: 138,200,016-138,200,016 ARMC8
    nsv5098687mobile element insertion1nstd203human GRCh38 chr3: 138,280,651-138,280,665 , GRCh37.p13 chr3: 137,999,493-137,999,507 NME9, ARMC8
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