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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973528insertion1nstd209human GRCh38 chr13: 71,118,130-71,118,130 , GRCh37.p13 chr13: 71,692,262-71,692,262 LINC00348
    nsv5936265copy number variation1nstd209human GRCh38 chr13: 71,022,567-71,022,696 , GRCh37.p13 chr13: 71,596,699-71,596,828 LINC00348
    nsv5931975copy number variation1nstd209human GRCh38 chr13: 71,122,860-71,122,936 , GRCh37.p13 chr13: 71,696,992-71,697,068 LINC00348
    nsv5929861copy number variation1nstd209human GRCh38 chr13: 71,118,978-71,119,077 , GRCh37.p13 chr13: 71,693,110-71,693,209 LINC00348
    nsv5849461copy number variation1nstd209human GRCh38 chr13: 71,019,412-71,021,688 , GRCh37.p13 chr13: 71,593,544-71,595,820 LINC00348
    nsv5725308mobile element insertion2nstd211human GRCh38 chr13: 71,076,246-71,076,246 , GRCh37.p13 chr13: 71,650,378-71,650,378 LINC00348
    nsv5714119mobile element insertion1nstd211human GRCh38 chr13: 71,137,760-71,137,760 , GRCh37.p13 chr13: 71,711,892-71,711,892 LINC00348
    nsv5712833mobile element insertion2nstd211human GRCh38 chr13: 71,055,126-71,055,126 , GRCh37.p13 chr13: 71,629,258-71,629,258 LINC00348
    nsv5652890insertion1nstd207human GRCh38 chr13: 71,118,095-71,118,095 , GRCh37.p13 chr13: 71,692,227-71,692,227 LINC00348
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5507061copy number variation1nstd206human GRCh38 chr13: 71,122,860-71,122,937 , GRCh37.p13 chr13: 71,696,992-71,697,069 LINC00348
    nsv5505368copy number variation1nstd206human GRCh38 chr13: 71,160,678-71,160,915 , GRCh37.p13 chr13: 71,734,810-71,735,047 LINC00348
    nsv5498740copy number variation1nstd206human GRCh38 chr13: 71,102,917-71,103,087 , GRCh37.p13 chr13: 71,677,049-71,677,219 LINC00348
    nsv5496191copy number variation1nstd206human GRCh38 chr13: 71,130,655-71,130,835 , GRCh37.p13 chr13: 71,704,787-71,704,967 LINC00348
    nsv5494962copy number variation1nstd206human GRCh38 chr13: 71,118,158-71,119,163 , GRCh37.p13 chr13: 71,692,290-71,693,295 LINC00348
    nsv5421009mobile element insertion1nstd206human GRCh38 chr13: 71,055,126-71,055,177 , GRCh37.p13 chr13: 71,629,258-71,629,309 LINC00348
    nsv5307600copy number variation1nstd204human GRCh38.p13 chr13: 67,378,459-71,217,205 , GRCh37.p13 chr13: 67,952,591-71,791,337 SRSF1P1, RN7SL761P, 32 more genes
    nsv5301005copy number variation1nstd204human GRCh38.p13 chr13: 71,061,955-71,128,917 , GRCh37.p13 chr13: 71,636,087-71,703,049 LINC00348
    nsv5278081copy number variation1nstd204human GRCh38.p13 chr13: 71,107,901-71,111,800 , GRCh37.p13 chr13: 71,682,033-71,685,932 LINC00348
    nsv5275213copy number variation1nstd204human GRCh38.p13 chr13: 71,078,450-71,079,849 , GRCh37.p13 chr13: 71,652,582-71,653,981 LINC00348
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