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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
    nsv5945843copy number variation1nstd209human GRCh38 chr14: 59,364,696-59,364,764 , GRCh37.p13 chr14: 59,831,414-59,831,482 DAAM1
    nsv5945237copy number variation1nstd209human GRCh38 chr14: 59,311,538-59,311,602 , GRCh37.p13 chr14: 59,778,256-59,778,320 DAAM1
    nsv5942935copy number variation1nstd209human GRCh38 chr14: 59,266,170-59,266,252 , GRCh37.p13 chr14: 59,732,888-59,732,970 DAAM1
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5723253mobile element insertion2nstd211human GRCh38 chr14: 59,347,117-59,347,117 , GRCh37.p13 chr14: 59,813,835-59,813,835 DAAM1
    nsv5719435mobile element insertion1nstd211human GRCh38 chr14: 59,229,629-59,229,629 , GRCh37.p13 chr14: 59,696,347-59,696,347 DAAM1
    nsv5708497mobile element insertion2nstd211human GRCh38 chr14: 59,316,281-59,316,281 , GRCh37.p13 chr14: 59,782,999-59,782,999 DAAM1
    nsv5703031mobile element insertion2nstd211human GRCh38 chr14: 59,243,319-59,243,319 , GRCh37.p13 chr14: 59,710,037-59,710,037 DAAM1
    nsv5655167insertion1nstd207human GRCh38 chr14: 59,243,307-59,243,307 , GRCh37.p13 chr14: 59,710,025-59,710,025 DAAM1
    nsv5648917insertion1nstd207human GRCh38 chr14: 59,289,767-59,289,767 , GRCh37.p13 chr14: 59,756,485-59,756,485 DAAM1
    nsv5561974mobile element insertion1nstd206human GRCh38 chr14: 59,229,629-59,229,680 , GRCh37.p13 chr14: 59,696,347-59,696,398 DAAM1
    nsv5511235copy number variation1nstd206human GRCh38 chr14: 59,344,401-59,344,490 , GRCh37.p13 chr14: 59,811,119-59,811,208 DAAM1
    nsv5505528copy number variation1nstd206human GRCh38 chr14: 59,366,135-59,366,328 , GRCh37.p13 chr14: 59,832,853-59,833,046 DAAM1
    nsv5504222copy number variation1nstd206human GRCh38 chr14: 59,311,540-59,311,603 , GRCh37.p13 chr14: 59,778,258-59,778,321 DAAM1
    nsv5501714copy number variation1nstd206human GRCh38 chr14: 59,327,217-59,327,332 , GRCh37.p13 chr14: 59,793,935-59,794,050 DAAM1
    nsv5495329copy number variation1nstd206human GRCh38 chr14: 59,364,937-59,364,999 , GRCh37.p13 chr14: 59,831,655-59,831,717 DAAM1
    nsv5430188mobile element insertion1nstd206human GRCh38 chr14: 59,243,319-59,243,370 , GRCh37.p13 chr14: 59,710,037-59,710,088 DAAM1
    nsv5427279mobile element insertion1nstd206human GRCh38 chr14: 59,316,281-59,316,332 , GRCh37.p13 chr14: 59,782,999-59,783,050 DAAM1
    nsv5357293translocation1nstd200human GRCh38 chr14: 59,311,540-59,311,540 , GRCh38 chr14: 59,311,603-59,311,603 , GRCh37.p13 chr14: 59,778,258-59,778,258 , GRCh37.p13 chr14: 59,778,321-59,778,321 DAAM1
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