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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6684617copy number variation1nstd229human GRCh38 chr2: 224,391,801-224,410,000 , GRCh37.p13 chr2: 225,256,518-225,274,717 FAM124B
    nsv6692434copy number variation1nstd229human GRCh38 chr2: 224,375,226-224,384,257 , GRCh37.p13 chr2: 225,239,943-225,248,974 FAM124B
    nsv6680934copy number variation1nstd229human GRCh38 chr2: 224,384,801-224,387,500 , GRCh37.p13 chr2: 225,249,518-225,252,217 FAM124B
    nsv6678330copy number variation1nstd229human GRCh38 chr2: 224,376,100-224,378,148 , GRCh37.p13 chr2: 225,240,817-225,242,865 FAM124B
    nsv6351093copy number variation1nstd223human GRCh38 chr2: 224,376,100-224,378,144 , GRCh37.p13 chr2: 225,240,817-225,242,861 FAM124B
    nsv5447837copy number variation1nstd206human GRCh38 chr2: 224,376,100-224,378,144 , GRCh37.p13 chr2: 225,240,817-225,242,861 FAM124B
    nsv5447239copy number variation1nstd206human GRCh38 chr2: 224,396,908-224,397,094 , GRCh37.p13 chr2: 225,261,625-225,261,811 FAM124B
    nsv5452767copy number variation1nstd206human GRCh38 chr2: 224,392,934-224,393,022 , GRCh37.p13 chr2: 225,257,651-225,257,739 FAM124B
    nsv4659248copy number variation1nstd186human GRCh37 chr2: 225,240,814-225,242,861 , GRCh38.p12 chr2: 224,376,097-224,378,144 FAM124B
    nsv4084157copy number variation1nstd166human GRCh37.p13 chr2: 225,262,947-225,266,257 , GRCh38.p12 chr2: 224,398,230-224,401,540 FAM124B
    nsv4076857copy number variation1nstd166human GRCh37.p13 chr2: 225,240,817-225,242,861 , GRCh38.p12 chr2: 224,376,100-224,378,144 FAM124B
    nsv4583412copy number variation1nstd183human GRCh37 chr2: 225,240,814-225,242,861 , GRCh38.p12 chr2: 224,376,097-224,378,144 FAM124B
    nsv4410960copy number variation1nstd174human GRCh37 chr2: 225,240,814-225,242,861 , GRCh38.p12 chr2: 224,376,097-224,378,144 FAM124B
    nsv1316915copy number variation1nstd122human NCBI36 chr2: 224,975,244-225,002,142 , GRCh37.p13 chr2: 225,267,000-225,293,898 , GRCh38.p12 chr2: 224,402,283-224,429,181 FAM124B
    esv3828363copy number variation2estd219human GRCh37 chr2: 225,240,503-225,243,193 , GRCh38.p12 chr2: 224,375,786-224,378,476 FAM124B
    esv3594467copy number variation2estd214human GRCh37 chr2: 225,240,503-225,243,193 , GRCh38.p12 chr2: 224,375,786-224,378,476 FAM124B
    esv3027298copy number variation1estd209human GRCh37 chr2: 225,257,525-225,257,527 , GRCh38.p12 chr2: 224,392,808-224,392,810 FAM124B
    esv3027297copy number variation1estd209human GRCh37 chr2: 225,253,253-225,253,254 , GRCh38.p12 chr2: 224,388,536-224,388,537 FAM124B
    esv2674413copy number variation1estd199human GRCh37 chr2: 225,240,814-225,242,861 , GRCh38.p12 chr2: 224,376,097-224,378,144 FAM124B
    esv3444417copy number variation1estd59human NCBI36 chr2: 224,957,853-224,959,070 , GRCh37.p13 chr2: 225,249,609-225,250,826 , GRCh38.p12 chr2: 224,384,892-224,386,109 FAM124B
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