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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5927371copy number variation1nstd209human GRCh38 chr10: 132,435,834-132,436,490 , GRCh37.p13 chr10: 134,249,338-134,249,994 LINC03068
    nsv5922613copy number variation1nstd209human GRCh38 chr10: 132,440,211-132,440,748 , GRCh37.p13 chr10: 134,253,715-134,254,252 LINC03068
    nsv5916827copy number variation1nstd209human GRCh38 chr10: 132,440,750-132,440,811 , GRCh37.p13 chr10: 134,254,254-134,254,315 LINC03068
    nsv5863026copy number variation1nstd209human GRCh38 chr10: 132,436,899-132,440,712 , GRCh37.p13 chr10: 134,250,403-134,254,216 LINC03068
    nsv5702489mobile element insertion1nstd211human GRCh38 chr10: 132,442,237-132,442,237 , GRCh37.p13 chr10: 134,255,741-134,255,741 LINC03068
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5637607insertion1nstd207human GRCh38 chr10: 132,440,344-132,440,344 , GRCh37.p13 chr10: 134,253,848-134,253,848 LINC03068
    nsv5637554insertion1nstd207human GRCh38 chr10: 132,436,099-132,436,099 , GRCh37.p13 chr10: 134,249,603-134,249,603 LINC03068
    nsv5634638insertion1nstd207human GRCh38 chr10: 132,440,346-132,440,346 , GRCh37.p13 chr10: 134,253,850-134,253,850 LINC03068
    nsv5631828insertion1nstd207human GRCh38 chr10: 132,440,569-132,440,569 , GRCh37.p13 chr10: 134,254,073-134,254,073 LINC03068
    nsv5626656insertion1nstd207human GRCh38 chr10: 132,440,593-132,440,593 , GRCh37.p13 chr10: 134,254,097-134,254,097 LINC03068
    nsv5603209copy number variation1nstd207human GRCh38 chr10: 132,440,677-132,440,749 , GRCh37.p13 chr10: 134,254,181-134,254,253 LINC03068
    nsv5603208copy number variation1nstd207human GRCh38 chr10: 132,440,275-132,440,712 , GRCh37.p13 chr10: 134,253,779-134,254,216 LINC03068
    nsv5601643copy number variation1nstd207human GRCh38 chr10: 132,440,346-132,440,545 , GRCh37.p13 chr10: 134,253,850-134,254,049 LINC03068
    nsv5598573copy number variation1nstd207human GRCh38 chr10: 132,440,450-132,440,514 , GRCh37.p13 chr10: 134,253,954-134,254,018 LINC03068
    nsv5593220copy number variation1nstd207human GRCh38 chr10: 132,436,099-132,436,186 , GRCh37.p13 chr10: 134,249,603-134,249,690 LINC03068
    nsv5508290copy number variation1nstd206human GRCh38 chr10: 132,437,837-132,438,071 , GRCh37.p13 chr10: 134,251,341-134,251,575 LINC03068
    nsv5504392copy number variation1nstd206human GRCh38 chr10: 132,435,835-132,436,508 , GRCh37.p13 chr10: 134,249,339-134,250,012 LINC03068
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