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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883302copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,606,092-47,614,167 , GRCh38 chr2: 47,378,953-47,387,028 EPCAM
    nsv4681931copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,606,078-47,613,752 , GRCh38.p12 chr2: 47,378,939-47,386,613 EPCAM
    nsv4728641copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,607,109-47,614,168 , GRCh38.p12 chr2: 47,379,970-47,387,029 EPCAM
    nsv4682291copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,612,194-47,618,236 , GRCh38.p12 chr2: 47,385,055-47,391,097 EPCAM
    nsv6311687copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 47,596,645-47,602,448 , GRCh38.p12 chr2: 47,369,506-47,375,309 EPCAM
    nsv5673447copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,383,698-47,388,606 , GRCh37 chr2: 47,610,837-47,615,745 EPCAM
    nsv6311408copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,612,824-47,615,711 , GRCh38.p12 chr2: 47,385,685-47,388,572 EPCAM
    nsv3889898copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,385,166-47,387,028 , GRCh37 chr2: 47,612,305-47,614,167 EPCAM
    nsv4450413copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,612,295-47,613,762 , GRCh38 chr2: 47,385,156-47,386,623 EPCAM
    nsv5564326copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,606,089-47,606,481 , GRCh38 chr2: 47,378,950-47,379,342 EPCAM
    nsv3882412copy number variation2nstd102humanUncertain significance, Pathogenic GRCh38 chr2: 47,369,496-47,369,591 , GRCh37 chr2: 47,596,635-47,596,730 EPCAM
    nsv5564417copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,385,164-47,385,253 , GRCh37 chr2: 47,612,303-47,612,392 EPCAM
    nsv3875589copy number variation1nstd102humanPathogenic GRCh38 chr2: 47,369,500-47,369,587 , GRCh37 chr2: 47,596,639-47,596,726 EPCAM
    nsv6311407copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,602,363-47,602,448 , GRCh38.p12 chr2: 47,375,224-47,375,309 EPCAM
    nsv4681812copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 47,596,645-47,596,730 , GRCh38.p12 chr2: 47,369,506-47,369,591 EPCAM
    nsv6311409copy number variation1nstd102humanPathogenic GRCh37 chr2: 47,613,701-47,613,752 , GRCh38.p12 chr2: 47,386,562-47,386,613 EPCAM
    nsv4681248copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 47,612,295-47,613,752 , GRCh38.p12 chr2: 47,385,156-47,386,613 EPCAM
    nsv6290227copy number variation1nstd102humannot provided GRCh37 chr2: 47,610,875-47,615,785 , GRCh38 chr2: 47,383,736-47,388,646 EPCAM
    nsv6315121copy number variation1nstd102humanUncertain significance GRCh37 chr2: 47,596,321-47,600,601 , GRCh38.p12 chr2: 47,369,182-47,373,462 EPCAM
    nsv4683558copy number variation1nstd102humanUncertain significance GRCh37 chr2: 47,606,898-47,607,118 , GRCh38.p12 chr2: 47,379,759-47,379,979 EPCAM
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