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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5892629copy number variation1nstd209human GRCh38 chr5: 179,677,331-179,677,811 , GRCh37.p13 chr5: 179,104,332-179,104,812 CANX, CBY3
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 LTC4S, MIR340, 28 more genes
    nsv5473019copy number variation1nstd206human GRCh38 chr5: 179,675,147-179,676,610 , GRCh37.p13 chr5: 179,102,148-179,103,611 CBY3
    nsv5470777copy number variation1nstd206human GRCh38 chr5: 179,680,424-179,680,474 , GRCh37.p13 chr5: 179,107,425-179,107,475 CANX, CBY3
    nsv5460387copy number variation1nstd206human GRCh38 chr5: 179,677,513-179,677,927 , GRCh37.p13 chr5: 179,104,514-179,104,928 CANX, CBY3
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377762, LOC105377759, 21 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100502572, C5orf60, 21 more genes
    nsv5301596copy number variation1nstd204human GRCh38.p13 chr5: 179,616,292-180,442,361 , GRCh37.p13 chr5: 179,043,293-179,869,361 MIR1229, MAPK9, 25 more genes
    nsv5238795copy number variation1nstd204human GRCh37.p13 chr5: 179,084,702-179,213,801 , GRCh38.p13 chr5: 179,657,701-179,786,800 CANX, MAML1, 4 more genes
    nsv5233947copy number variation1nstd204human GRCh38.p13 chr5: 179,616,201-179,907,500 , GRCh37.p13 chr5: 179,043,202-179,334,500 CBY3, LOC100502572, 15 more genes
    nsv5231078copy number variation1nstd204human GRCh37.p13 chr5: 179,071,502-179,120,301 , GRCh38.p13 chr5: 179,644,501-179,693,300 CANX, C5orf60, 4 more genes
    nsv5229255copy number variation1nstd204human GRCh38.p13 chr5: 179,661,860-179,687,252 , GRCh37.p13 chr5: 179,088,861-179,114,253 CANX, CBY3, 1 more genes
    nsv5223579copy number variation1nstd204human GRCh38.p13 chr5: 179,677,760-179,727,134 , GRCh37.p13 chr5: 179,104,761-179,154,135 CBY3, HMGB3P22, 1 more genes
    nsv4940114copy number variation1nstd200human GRCh38 chr5: 178,985,568-179,789,759 , GRCh37.p13 chr5: 178,412,569-179,216,760 , LOC100884169, 21 more genes
    nsv4826127copy number variation1nstd200human GRCh37 chr5: 179,104,352-179,104,816 , GRCh38.p12 chr5: 179,677,351-179,677,815 , GRCh38.p12 chr5|NW_016107298.1: 443,038-443,502 CANX, CBY3
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4675130copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,487,249-180,622,216 , GRCh38.p12 chr5: 179,060,248-181,195,216 OR2V2, TRV-AAC1-2, 81 more genes
    nsv4567769sequence alteration1nstd166human GRCh37.p13 chr5: 179,087,898-179,119,724 , GRCh38.p12 chr5: 179,660,897-179,692,723 , GRCh38.p12 chr5|NW_016107298.1: 426,603-458,421 CANX, CBY3, 2 more genes
    nsv4522700copy number variation1nstd166human GRCh37.p13 chr5: 179,102,721-179,140,011 , GRCh38.p12 chr5: 179,675,720-179,713,010 , GRCh38.p12 chr5|NW_016107298.1: 441,423-478,589 CANX, CBY3, 1 more genes
    nsv4455497copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,848,982-180,719,789 , GRCh38.p12 chr5: 177,421,981-181,292,788 HEIH, MGAT4B, 149 more genes
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