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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6716772copy number variation1nstd229human GRCh38 chr3: 49,140,954-49,160,821 , GRCh37.p13 chr3: 49,178,387-49,198,254 LAMB2P1, CCDC71
    nsv6705373copy number variation1nstd229human GRCh38 chr3: 49,160,157-49,160,658 , GRCh37.p13 chr3: 49,197,590-49,198,091 CCDC71
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6372055copy number variation1nstd223human GRCh38 chr3: 48,386,801-49,230,000 , GRCh37.p13 chr3: 48,428,291-49,267,433 NCKIPSD, UCN2, 44 more genes
    nsv6365655copy number variation1nstd223human GRCh38 chr3: 49,160,330-49,160,639 , GRCh37.p13 chr3: 49,197,763-49,198,072 CCDC71
    nsv6313476copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,060,512-49,678,685 , GRCh38.p12 chr3: 49,023,079-49,641,252 DAG1, GPX1, 23 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 more genes
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5993721copy number variation1nstd212human GRCh38 chr3: 49,160,319-49,160,641 , GRCh37.p13 chr3: 49,197,752-49,198,074 CCDC71
    nsv5901423copy number variation1nstd209human GRCh38 chr3: 49,163,183-49,163,290 , GRCh37.p13 chr3: 49,200,616-49,200,723 CCDC71
    nsv5887936copy number variation1nstd209human GRCh38 chr3: 49,160,316-49,160,638 , GRCh37.p13 chr3: 49,197,749-49,198,071 CCDC71
    nsv5673729copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,507,870-50,340,407 , GRCh38.p12 chr3: 48,466,471-50,302,976 SEMA3B-AS1, GNAT1, 87 more genes
    nsv5565296copy number variation1nstd207human GRCh38 chr3: 49,160,316-49,160,638 , GRCh37.p13 chr3: 49,197,749-49,198,071 CCDC71
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5444416copy number variation1nstd206human GRCh38 chr3: 49,160,330-49,160,639 , GRCh37.p13 chr3: 49,197,763-49,198,072 CCDC71
    nsv5382705mobile element deletion2nstd186human GRCh37 chr3: 49,197,763-49,198,072 , GRCh38.p12 chr3: 49,160,330-49,160,639 CCDC71
    nsv5211625mobile element deletion1nstd204human GRCh38.p13 chr3: 49,160,330-49,160,639 , GRCh37.p13 chr3: 49,197,763-49,198,072 CCDC71
    nsv5211134copy number variation1nstd204human GRCh38.p13 chr3: 48,639,801-49,381,300 , GRCh37.p13 chr3: 48,677,234-49,418,733 MIR6890, IHO1, 31 more genes
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
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