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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6123023copy number variation1nstd186human GRCh37 chr13: 36,806,787-36,806,861 , GRCh38.p12 chr13: 36,232,650-36,232,724 CCDC169-SOHLH2, CCDC169
    nsv5971384insertion1nstd209human GRCh38 chr13: 36,184,460-36,184,460 , GRCh37.p13 chr13: 36,758,597-36,758,597 CCDC169-SOHLH2, SOHLH2
    nsv5944998copy number variation1nstd209human GRCh38 chr13: 36,244,777-36,244,837 , GRCh37.p13 chr13: 36,818,914-36,818,974 CCDC169-SOHLH2, CCDC169
    nsv5944241copy number variation1nstd209human GRCh38 chr13: 36,217,729-36,221,511 , GRCh37.p13 chr13: 36,791,866-36,795,648 CCDC169-SOHLH2, CCDC169
    nsv5938589copy number variation1nstd209human GRCh38 chr13: 36,164,582-36,167,387 , GRCh37.p13 chr13: 36,738,719-36,741,524 SOHLH2, CCDC169-SOHLH2
    nsv5929481copy number variation1nstd209human GRCh38 chr13: 36,232,633-36,232,723 , GRCh37.p13 chr13: 36,806,770-36,806,860 CCDC169, CCDC169-SOHLH2
    nsv5862296copy number variation1nstd209human GRCh38 chr13: 36,164,571-36,167,212 , GRCh37.p13 chr13: 36,738,708-36,741,349 SOHLH2, CCDC169-SOHLH2
    nsv5848698copy number variation1nstd209human GRCh38 chr13: 36,217,780-36,221,179 , GRCh37.p13 chr13: 36,791,917-36,795,316 CCDC169, CCDC169-SOHLH2
    nsv5848403copy number variation1nstd209human GRCh38 chr13: 36,185,263-36,188,112 , GRCh37.p13 chr13: 36,759,400-36,762,249 CCDC169-SOHLH2, SOHLH2
    nsv5603451copy number variation1nstd207human GRCh38 chr13: 36,244,777-36,244,837 , GRCh37.p13 chr13: 36,818,914-36,818,974 CCDC169, CCDC169-SOHLH2
    nsv5587783copy number variation1nstd207human GRCh38 chr13: 36,232,633-36,232,723 , GRCh37.p13 chr13: 36,806,770-36,806,860 CCDC169-SOHLH2, CCDC169
    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
    nsv5513848copy number variation1nstd206human GRCh38 chr13: 36,279,283-36,281,365 , GRCh37.p13 chr13: 36,853,420-36,855,502 CCDC169-SOHLH2, CCDC169
    nsv5512182copy number variation1nstd206human GRCh38 chr13: 36,217,729-36,221,512 , GRCh37.p13 chr13: 36,791,866-36,795,649 CCDC169, CCDC169-SOHLH2
    nsv5503810copy number variation1nstd206human GRCh38 chr13: 36,226,805-36,237,327 , GRCh37.p13 chr13: 36,800,942-36,811,464 CCDC169-SOHLH2, CCDC169
    nsv5502145copy number variation1nstd206human GRCh38 chr13: 36,224,496-36,228,037 , GRCh37.p13 chr13: 36,798,633-36,802,174 CCDC169-SOHLH2, CCDC169
    nsv5499363copy number variation1nstd206human GRCh38 chr13: 36,232,650-36,232,724 , GRCh37.p13 chr13: 36,806,787-36,806,861 CCDC169, CCDC169-SOHLH2
    nsv5356778translocation1nstd200human GRCh38 chr13: 36,291,964-36,291,964 , GRCh38 chr13: 36,292,033-36,292,033 , GRCh37.p13 chr13: 36,866,101-36,866,101 , GRCh37.p13 chr13: 36,866,170-36,866,170 CCDC169, CCDC169-SOHLH2
    nsv5356777translocation1nstd200human GRCh38 chr13: 36,240,442-36,240,442 , GRCh38 chr13: 36,240,363-36,240,363 , GRCh37.p13 chr13: 36,814,500-36,814,500 , GRCh37.p13 chr13: 36,814,579-36,814,579 CCDC169-SOHLH2, CCDC169
    nsv5356776translocation1nstd200human GRCh38 chr13: 36,232,724-36,232,724 , GRCh38 chr13: 36,232,650-36,232,650 , GRCh37.p13 chr13: 36,806,861-36,806,861 , GRCh37.p13 chr13: 36,806,787-36,806,787 CCDC169, CCDC169-SOHLH2
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