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Items: 1 to 20 of 986

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957345insertion1nstd209human GRCh38 chr7: 132,166,351-132,166,351 , GRCh37.p13 chr7: 131,851,110-131,851,110 PLXNA4
    nsv5950052insertion1nstd209human GRCh38 chr7: 132,179,267-132,179,267 , GRCh37.p13 chr7: 131,864,026-131,864,026 PLXNA4
    nsv5949754insertion1nstd209human GRCh38 chr7: 132,334,560-132,334,560 , GRCh37.p13 chr7: 132,019,319-132,019,319 PLXNA4
    nsv5947608insertion1nstd209human GRCh38 chr7: 132,608,124-132,608,124 , GRCh37.p13 chr7: 132,292,883-132,292,883 PLXNA4
    nsv5925458copy number variation1nstd209human GRCh38 chr7: 132,115,919-132,124,896 , GRCh37.p13 chr7: 131,800,678-131,809,655 PLXNA4
    nsv5920185copy number variation1nstd209human GRCh38 chr7: 132,562,069-132,562,986 , GRCh37.p13 chr7: 132,246,828-132,247,745 PLXNA4
    nsv5917559copy number variation1nstd209human GRCh38 chr7: 132,319,415-132,319,471 , GRCh37.p13 chr7: 132,004,174-132,004,230 PLXNA4
    nsv5917144copy number variation1nstd209human GRCh38 chr7: 132,317,402-132,317,466 , GRCh37.p13 chr7: 132,002,161-132,002,225 PLXNA4
    nsv5916806copy number variation1nstd209human GRCh38 chr7: 132,588,252-132,588,783 , GRCh37.p13 chr7: 132,273,011-132,273,542 PLXNA4
    nsv5916677copy number variation1nstd209human GRCh38 chr7: 132,598,582-132,598,660 , GRCh37.p13 chr7: 132,283,341-132,283,419 PLXNA4
    nsv5916345copy number variation1nstd209human GRCh38 chr7: 132,607,898-132,608,047 , GRCh37.p13 chr7: 132,292,657-132,292,806 PLXNA4
    nsv5915051copy number variation1nstd209human GRCh38 chr7: 132,404,161-132,404,863 , GRCh37.p13 chr7: 132,088,920-132,089,622 LOC105375511, PLXNA4
    nsv5914309copy number variation1nstd209human GRCh38 chr7: 132,132,398-132,132,467 , GRCh37.p13 chr7: 131,817,157-131,817,226 PLXNA4
    nsv5913726copy number variation1nstd209human GRCh38 chr7: 132,225,949-132,226,011 , GRCh37.p13 chr7: 131,910,708-131,910,770 PLXNA4
    nsv5910813copy number variation1nstd209human GRCh38 chr7: 132,480,477-132,480,573 , GRCh37.p13 chr7: 132,165,236-132,165,332 PLXNA4
    nsv5910129copy number variation1nstd209human GRCh38 chr7: 132,238,687-132,239,509 , GRCh37.p13 chr7: 131,923,446-131,924,268 PLXNA4
    nsv5909525copy number variation1nstd209human GRCh38 chr7: 132,322,212-132,323,340 , GRCh37.p13 chr7: 132,006,971-132,008,099 PLXNA4
    nsv5867532copy number variation1nstd209human GRCh38 chr7: 132,280,352-132,283,235 , GRCh37.p13 chr7: 131,965,111-131,967,994 PLXNA4
    nsv5862637copy number variation2nstd209human GRCh38 chr7: 132,281,352-132,283,385 , GRCh37.p13 chr7: 131,966,111-131,968,144 PLXNA4
    nsv5861691copy number variation1nstd209human GRCh38 chr7: 132,115,891-132,124,934 , GRCh37.p13 chr7: 131,800,650-131,809,693 PLXNA4
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