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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3896109copy number variation1nstd102humanBenign GRCh37 chr14: 104,554,921-104,566,119 , GRCh38.p12 chr14: 104,088,584-104,099,782 ASPG
    nsv6976130copy number variation1nstd229human GRCh38 chr14: 104,087,901-104,093,772 , GRCh37.p13 chr14: 104,554,238-104,560,109 ASPG
    nsv6960580copy number variation1nstd229human GRCh38 chr14: 104,095,892-104,099,131 , GRCh37.p13 chr14: 104,562,229-104,565,468 ASPG
    nsv6963114copy number variation1nstd229human GRCh38 chr14: 104,092,139-104,094,058 , GRCh37.p13 chr14: 104,558,476-104,560,395 ASPG
    nsv6959662copy number variation1nstd229human GRCh38 chr14: 104,093,653-104,093,692 , GRCh37.p13 chr14: 104,559,990-104,560,029 ASPG
    nsv6505717copy number variation1nstd223human GRCh38 chr14: 104,087,899-104,093,764 , GRCh37.p13 chr14: 104,554,236-104,560,101 ASPG
    nsv6500356copy number variation1nstd223human GRCh38 chr14: 104,112,141-104,112,531 , GRCh37.p13 chr14: 104,578,478-104,578,868 ASPG
    nsv5509508copy number variation1nstd206human GRCh38 chr14: 104,087,874-104,093,786 , GRCh37.p13 chr14: 104,554,211-104,560,123 ASPG
    nsv6202783copy number variation1nstd214human GRCh38 chr14: 104,098,008-104,098,163 , GRCh37.p13 chr14: 104,564,345-104,564,500 ASPG
    nsv6189110copy number variation1nstd214human GRCh38 chr14: 104,097,826-104,097,981 , GRCh37.p13 chr14: 104,564,163-104,564,318 ASPG
    nsv6200513copy number variation1nstd214human GRCh38 chr14: 104,097,917-104,098,046 , GRCh37.p13 chr14: 104,564,254-104,564,383 ASPG
    nsv6188216copy number variation1nstd214human GRCh38 chr14: 104,093,665-104,093,777 , GRCh37.p13 chr14: 104,560,002-104,560,114 ASPG
    nsv6202559copy number variation1nstd214human GRCh38 chr14: 104,097,842-104,097,945 , GRCh37.p13 chr14: 104,564,179-104,564,282 ASPG
    nsv6194462copy number variation1nstd214human GRCh38 chr14: 104,097,826-104,097,929 , GRCh37.p13 chr14: 104,564,163-104,564,266 ASPG
    nsv6199250copy number variation1nstd214human GRCh38 chr14: 104,098,064-104,098,125 , GRCh37.p13 chr14: 104,564,401-104,564,462 ASPG
    nsv6205297copy number variation1nstd214human GRCh38 chr14: 104,097,809-104,097,860 , GRCh37.p13 chr14: 104,564,146-104,564,197 ASPG
    nsv6203110copy number variation1nstd214human GRCh38 chr14: 104,097,894-104,097,945 , GRCh37.p13 chr14: 104,564,231-104,564,282 ASPG
    nsv6023364copy number variation1nstd212human GRCh38 chr14: 104,097,989-104,098,104 , GRCh37.p13 chr14: 104,564,326-104,564,441 ASPG
    nsv6035016copy number variation1nstd212human GRCh38 chr14: 104,097,842-104,097,942 , GRCh37.p13 chr14: 104,564,179-104,564,279 ASPG
    nsv4744101copy number variation1nstd199human GRCh37 chr14: 104,564,156-104,564,257 , GRCh38.p12 chr14: 104,097,819-104,097,920 ASPG
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