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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889493copy number variation1nstd102humanBenign GRCh37 chr2: 56,580,537-56,784,574 , GRCh38.p12 chr2: 56,353,402-56,557,439 CCDC85A
    nsv6676515copy number variation1nstd229human GRCh38 chr2: 56,337,103-56,440,695 , GRCh37.p13 chr2: 56,564,238-56,667,830 CCDC85A
    nsv6669740copy number variation1nstd229human GRCh38 chr2: 56,244,282-56,295,770 , GRCh37.p13 chr2: 56,471,417-56,522,905 CCDC85A
    nsv6660036copy number variation1nstd229human GRCh38 chr2: 56,241,101-56,283,900 , GRCh37.p13 chr2: 56,468,236-56,511,035 CCDC85A
    nsv6667274copy number variation1nstd229human GRCh38 chr2: 56,295,573-56,327,892 , GRCh37.p13 chr2: 56,522,708-56,555,027 CCDC85A
    nsv6662701copy number variation1nstd229human GRCh38 chr2: 56,269,360-56,286,165 , GRCh37.p13 chr2: 56,496,495-56,513,300 CCDC85A
    nsv6669286copy number variation1nstd229human GRCh38 chr2: 56,203,614-56,218,894 , GRCh37.p13 chr2: 56,430,749-56,446,029 CCDC85A
    nsv6675599copy number variation1nstd229human GRCh38 chr2: 56,259,608-56,271,112 , GRCh37.p13 chr2: 56,486,743-56,498,247 CCDC85A
    nsv6664158copy number variation1nstd229human GRCh38 chr2: 56,361,949-56,370,706 , GRCh37.p13 chr2: 56,589,084-56,597,841 CCDC85A
    nsv6671740copy number variation1nstd229human GRCh38 chr2: 56,308,364-56,316,135 , GRCh37.p13 chr2: 56,535,499-56,543,270 CCDC85A
    nsv6674373copy number variation1nstd229human GRCh38 chr2: 56,223,323-56,230,655 , GRCh37.p13 chr2: 56,450,458-56,457,790 CCDC85A
    nsv6667044copy number variation1nstd229human GRCh38 chr2: 56,244,370-56,251,617 , GRCh37.p13 chr2: 56,471,505-56,478,752 CCDC85A
    nsv6665329copy number variation1nstd229human GRCh38 chr2: 56,333,135-56,339,937 , GRCh37.p13 chr2: 56,560,270-56,567,072 CCDC85A
    nsv6671883copy number variation1nstd229human GRCh38 chr2: 56,244,845-56,250,887 , GRCh37.p13 chr2: 56,471,980-56,478,022 CCDC85A
    nsv6662558copy number variation1nstd229human GRCh38 chr2: 56,216,116-56,221,668 , GRCh37.p13 chr2: 56,443,251-56,448,803 CCDC85A
    nsv6659558copy number variation1nstd229human GRCh38 chr2: 56,212,501-56,217,900 , GRCh37.p13 chr2: 56,439,636-56,445,035 CCDC85A
    nsv6672124copy number variation1nstd229human GRCh38 chr2: 56,288,601-56,293,900 , GRCh37.p13 chr2: 56,515,736-56,521,035 CCDC85A
    nsv6678021copy number variation1nstd229human GRCh38 chr2: 56,258,244-56,262,160 , GRCh37.p13 chr2: 56,485,379-56,489,295 CCDC85A
    nsv6672614copy number variation1nstd229human GRCh38 chr2: 56,310,378-56,314,007 , GRCh37.p13 chr2: 56,537,513-56,541,142 CCDC85A
    nsv6675079copy number variation1nstd229human GRCh38 chr2: 56,359,681-56,363,094 , GRCh37.p13 chr2: 56,586,816-56,590,229 CCDC85A
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