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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5944158copy number variation1nstd209human GRCh38 chr14: 54,891,481-54,897,080 , GRCh37.p13 chr14: 55,358,199-55,363,798 GCH1
    nsv5938956copy number variation1nstd209human GRCh38 chr14: 54,896,835-54,896,925 , GRCh37.p13 chr14: 55,363,553-55,363,643 GCH1
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5932303copy number variation1nstd209human GRCh38 chr14: 54,853,171-54,859,494 , GRCh37.p13 chr14: 55,319,889-55,326,212 GCH1, RNU6ATAC9P
    nsv5867375copy number variation1nstd209human GRCh38 chr14: 54,861,407-54,863,206 , GRCh37.p13 chr14: 55,328,125-55,329,924 GCH1
    nsv5866295copy number variation1nstd209human GRCh38 chr14: 54,853,262-54,859,386 , GRCh37.p13 chr14: 55,319,980-55,326,104 GCH1, RNU6ATAC9P
    nsv5865449copy number variation1nstd209human GRCh38 chr14: 54,891,421-54,896,820 , GRCh37.p13 chr14: 55,358,139-55,363,538 GCH1
    nsv5705406mobile element insertion1nstd211human GRCh38 chr14: 54,884,789-54,884,789 , GRCh37.p13 chr14: 55,351,507-55,351,507 FDPSP3, GCH1
    nsv5701855mobile element insertion1nstd211human GRCh38 chr14: 54,884,786-54,884,786 , GRCh37.p13 chr14: 55,351,504-55,351,504 FDPSP3, GCH1
    nsv5698649mobile element insertion1nstd211human GRCh38 chr14: 54,870,335-54,870,335 , GRCh37.p13 chr14: 55,337,053-55,337,053 GCH1
    nsv5672657copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,332,039-55,369,387 , GRCh38.p12 chr14: 54,865,321-54,902,669 GCH1, FDPSP3, 1 more genes
    nsv5672575copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,313,807-55,313,858 , GRCh38.p12 chr14: 54,847,089-54,847,140 GCH1
    nsv5596968copy number variation1nstd207human GRCh38 chr14: 54,880,680-54,880,739 , GRCh37.p13 chr14: 55,347,398-55,347,457 GCH1
    nsv5584640copy number variation1nstd207human GRCh38 chr14: 54,880,539-54,880,598 , GRCh37.p13 chr14: 55,347,257-55,347,316 GCH1
    nsv5535519insertion1nstd206human GRCh38 chr14: 54,868,447-54,868,483 , GRCh37.p13 chr14: 55,335,165-55,335,201 GCH1
    nsv5508455copy number variation1nstd206human GRCh38 chr14: 54,853,176-54,859,495 , GRCh37.p13 chr14: 55,319,894-55,326,213 RNU6ATAC9P, GCH1
    nsv5498043copy number variation1nstd206human GRCh38 chr14: 54,896,835-54,896,930 , GRCh37.p13 chr14: 55,363,553-55,363,648 GCH1
    nsv5497291copy number variation1nstd206human GRCh38 chr14: 54,861,688-54,863,358 , GRCh37.p13 chr14: 55,328,406-55,330,076 GCH1
    nsv5496707copy number variation1nstd206human GRCh38 chr14: 54,897,575-54,900,077 , GRCh37.p13 chr14: 55,364,293-55,366,795 GCH1
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