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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
    nsv5979955insertion1nstd209human GRCh38 chr10: 124,788,710-124,788,710 , GRCh37.p13 chr10: 126,477,279-126,477,279 EEF1AKMT2
    nsv5977616insertion1nstd209human GRCh38 chr10: 124,769,233-124,769,233 , GRCh37.p13 chr10: 126,457,802-126,457,802 EEF1AKMT2
    nsv5908969copy number variation1nstd209human GRCh38 chr10: 124,766,989-124,771,696 , GRCh37.p13 chr10: 126,455,558-126,460,265 EEF1AKMT2
    nsv5867317copy number variation1nstd209human GRCh38 chr10: 124,767,591-124,771,668 , GRCh37.p13 chr10: 126,456,160-126,460,237 EEF1AKMT2
    nsv5706043mobile element insertion2nstd211human GRCh38 chr10: 124,761,414-124,761,414 , GRCh37.p13 chr10: 126,449,983-126,449,983 EEF1AKMT2
    nsv5634578insertion1nstd207human GRCh38 chr10: 124,761,401-124,761,401 , GRCh37.p13 chr10: 126,449,970-126,449,970 EEF1AKMT2
    nsv5560549sequence alteration1nstd206human GRCh38 chr10: 124,782,440-124,782,536 , GRCh37.p13 chr10: 126,471,009-126,471,105 EEF1AKMT2
    nsv5548445insertion1nstd206human GRCh38 chr10: 124,784,052-124,784,102 , GRCh37.p13 chr10: 126,472,621-126,472,671 EEF1AKMT2
    nsv5512881copy number variation1nstd206human GRCh38 chr10: 124,787,000-124,793,502 , GRCh37.p13 chr10: 126,475,569-126,482,071 EEF1AKMT2
    nsv5502212copy number variation1nstd206human GRCh38 chr10: 124,771,502-124,783,502 , GRCh37.p13 chr10: 126,460,071-126,472,071 EEF1AKMT2
    nsv5395924mobile element insertion1nstd206human GRCh38 chr10: 124,761,401-124,761,401 , GRCh37.p13 chr10: 126,449,970-126,449,970 EEF1AKMT2
    nsv5199472mobile element insertion1nstd203human GRCh38 chr10: 124,780,749-124,780,763 , GRCh37.p13 chr10: 126,469,318-126,469,332 EEF1AKMT2
    nsv5137438mobile element insertion1nstd203human GRCh38 chr10: 124,761,406-124,761,414 , GRCh37.p13 chr10: 126,449,975-126,449,983 EEF1AKMT2
    nsv5128042mobile element insertion1nstd203human GRCh38 chr10: 124,761,401-124,761,414 , GRCh37.p13 chr10: 126,449,970-126,449,983 EEF1AKMT2
    nsv5124910mobile element insertion1nstd203human GRCh38 chr10: 124,769,218-124,769,234 , GRCh37.p13 chr10: 126,457,787-126,457,803 EEF1AKMT2
    nsv4983966copy number variation1nstd200human GRCh38 chr10: 124,783,330-124,804,950 , GRCh37.p13 chr10: 126,471,899-126,493,519 EEF1AKMT2, ABRAXAS2
    nsv4983965copy number variation1nstd200human GRCh38 chr10: 124,771,637-124,782,455 , GRCh37.p13 chr10: 126,460,206-126,471,024 EEF1AKMT2
    nsv4977390copy number variation1nstd200human GRCh38 chr10: 124,784,781-124,793,654 , GRCh37.p13 chr10: 126,473,350-126,482,223 EEF1AKMT2
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