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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976653inversion1nstd209human GRCh38 chr2: 10,740,038-10,740,749 , GRCh37.p13 chr2: 10,880,164-10,880,875 ATP6V1C2
    nsv5884333copy number variation1nstd209human GRCh38 chr2: 10,745,533-10,753,722 , GRCh37.p13 chr2: 10,885,659-10,893,848 ATP6V1C2
    nsv5876776copy number variation1nstd209human GRCh38 chr2: 10,782,060-10,782,112 , GRCh37.p13 chr2: 10,922,186-10,922,238 ATP6V1C2, PDIA6
    nsv5868260copy number variation1nstd209human GRCh38 chr2: 10,764,797-10,770,225 , GRCh37.p13 chr2: 10,904,923-10,910,351 LOC105373428, ATP6V1C2
    nsv5831161copy number variation1nstd209human GRCh38 chr2: 10,745,550-10,754,046 , GRCh37.p13 chr2: 10,885,676-10,894,172 ATP6V1C2
    nsv5831079copy number variation1nstd209human GRCh38 chr2: 10,764,838-10,770,087 , GRCh37.p13 chr2: 10,904,964-10,910,213 LOC105373428, ATP6V1C2
    nsv5830570copy number variation1nstd209human GRCh38 chr2: 10,747,247-10,749,246 , GRCh37.p13 chr2: 10,887,373-10,889,372 ATP6V1C2
    nsv5721745mobile element insertion1nstd211human GRCh38 chr2: 10,749,528-10,749,528 , GRCh37.p13 chr2: 10,889,654-10,889,654 ATP6V1C2
    nsv5720947mobile element insertion1nstd211human GRCh38 chr2: 10,749,540-10,749,540 , GRCh37.p13 chr2: 10,889,666-10,889,666 ATP6V1C2
    nsv5446203copy number variation1nstd206human GRCh38 chr2: 10,725,651-10,727,219 , GRCh37.p13 chr2: 10,865,777-10,867,345 ATP6V1C2
    nsv5444347copy number variation1nstd206human GRCh38 chr2: 10,755,229-10,755,354 , GRCh37.p13 chr2: 10,895,355-10,895,480 ATP6V1C2
    nsv5440446copy number variation1nstd206human GRCh38 chr2: 10,745,504-10,753,750 , GRCh37.p13 chr2: 10,885,630-10,893,876 ATP6V1C2
    nsv5438811copy number variation1nstd206human GRCh38 chr2: 10,782,060-10,782,113 , GRCh37.p13 chr2: 10,922,186-10,922,239 PDIA6, ATP6V1C2
    nsv5357919translocation1nstd200human GRCh38 chr2: 10,753,954-10,753,954 , GRCh38 chr2: 10,752,772-10,752,772 , GRCh37.p13 chr2: 10,894,080-10,894,080 , GRCh37.p13 chr2: 10,892,898-10,892,898 ATP6V1C2
    nsv5299677copy number variation1nstd204human GRCh38.p13 chr2: 10,759,722-10,760,093 , GRCh37.p13 chr2: 10,899,848-10,900,219 ATP6V1C2
    nsv5203130copy number variation1nstd204human GRCh38.p13 chr2: 10,742,824-10,745,349 , GRCh37.p13 chr2: 10,882,950-10,885,475 ATP6V1C2, RNU7-138P
    nsv5074104mobile element insertion1nstd203human GRCh38 chr2: 10,725,040-10,725,059 , GRCh37.p13 chr2: 10,865,166-10,865,185 ATP6V1C2
    nsv4904767copy number variation1nstd200human GRCh38 chr2: 10,761,971-10,782,965 , GRCh37.p13 chr2: 10,902,097-10,923,091 LOC105373428, ATP6V1C2, 1 more genes
    nsv4904766copy number variation1nstd200human GRCh38 chr2: 10,745,499-10,753,751 , GRCh37.p13 chr2: 10,885,625-10,893,877 ATP6V1C2
    nsv4900211copy number variation1nstd200human GRCh38 chr2: 10,776,689-10,776,844 , GRCh37.p13 chr2: 10,916,815-10,916,970 ATP6V1C2
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