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Items: 1 to 20 of 478

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122589copy number variation1nstd186human GRCh37 chr12: 94,669,348-94,669,655 , GRCh38.p12 chr12: 94,275,572-94,275,879 CEP83, PLXNC1
    nsv5969052insertion1nstd209human GRCh38 chr12: 94,274,155-94,274,155 , GRCh37.p13 chr12: 94,667,931-94,667,931 PLXNC1, CEP83
    nsv5947113copy number variation1nstd209human GRCh38 chr12: 94,275,556-94,275,878 , GRCh37.p13 chr12: 94,669,332-94,669,654 PLXNC1, CEP83
    nsv5933321copy number variation1nstd209human GRCh38 chr12: 94,165,580-94,166,312 , GRCh37.p13 chr12: 94,559,356-94,560,088 PLXNC1
    nsv5700908mobile element insertion2nstd211human GRCh38 chr12: 94,215,829-94,215,829 , GRCh37.p13 chr12: 94,609,605-94,609,605 PLXNC1
    nsv5604504copy number variation1nstd207human GRCh38 chr12: 94,275,556-94,275,878 , GRCh37.p13 chr12: 94,669,332-94,669,654 CEP83, PLXNC1
    nsv5598846copy number variation1nstd207human GRCh38 chr12: 94,177,133-94,177,200 , GRCh37.p13 chr12: 94,570,909-94,570,976 PLXNC1
    nsv5555893inversion1nstd206human GRCh38 chr12: 94,232,385-94,232,494 , GRCh37.p13 chr12: 94,626,161-94,626,270 PLXNC1
    nsv5512183copy number variation1nstd206human GRCh38 chr12: 94,275,572-94,275,879 , GRCh37.p13 chr12: 94,669,348-94,669,655 PLXNC1, CEP83
    nsv5510783copy number variation1nstd206human GRCh38 chr12: 94,235,775-94,235,837 , GRCh37.p13 chr12: 94,629,551-94,629,613 PLXNC1
    nsv5508743copy number variation1nstd206human GRCh38 chr12: 94,204,872-94,205,172 , GRCh37.p13 chr12: 94,598,648-94,598,948 PLXNC1
    nsv5505145copy number variation1nstd206human GRCh38 chr12: 94,217,156-94,217,350 , GRCh37.p13 chr12: 94,610,932-94,611,126 PLXNC1
    nsv5501172copy number variation1nstd206human GRCh38 chr12: 94,184,334-94,184,511 , GRCh37.p13 chr12: 94,578,110-94,578,287 PLXNC1
    nsv5497289copy number variation1nstd206human GRCh38 chr12: 94,165,580-94,166,313 , GRCh37.p13 chr12: 94,559,356-94,560,089 PLXNC1
    nsv5429724mobile element insertion1nstd206human GRCh38 chr12: 94,215,829-94,215,880 , GRCh37.p13 chr12: 94,609,605-94,609,656 PLXNC1
    nsv5383263mobile element deletion2nstd186human GRCh37 chr12: 94,669,348-94,669,655 , GRCh38.p12 chr12: 94,275,572-94,275,879 PLXNC1, CEP83
    nsv5380743copy number variation1nstd102humanUncertain significance GRCh37 chr12: 94,634,261-94,806,266 , GRCh38.p12 chr12: 94,240,485-94,412,490 CEP83, PLXNC1, 1 more genes
    nsv5380633translocation1nstd200human GRCh38 chr1: 30,931,506-30,931,506 , GRCh38 chr12: 94,168,519-94,168,519 , GRCh37.p13 chr1: 31,404,353-31,404,353 , GRCh37.p13 chr12: 94,562,295-94,562,295 PLXNC1, PUM1
    nsv5343420translocation1nstd200human GRCh37 chr1: 31,404,353-31,404,353 , GRCh37 chr12: 94,562,295-94,562,295 , GRCh38.p12 chr1: 30,931,506-30,931,506 , GRCh38.p12 chr12: 94,168,519-94,168,519 PUM1, PLXNC1
    nsv5332369translocation1nstd200human GRCh37 chr12: 94,560,089-94,560,089 , GRCh37 chr12: 94,559,356-94,559,356 , GRCh38.p12 chr12: 94,166,313-94,166,313 , GRCh38.p12 chr12: 94,165,580-94,165,580 PLXNC1
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