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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946315copy number variation1nstd209human GRCh38 chr17: 58,727,078-58,727,381 , GRCh37.p13 chr17: 56,804,439-56,804,742 LOC105371843, RAD51C
    nsv5941631copy number variation1nstd209human GRCh38 chr17: 58,712,549-58,712,850 , GRCh37.p13 chr17: 56,789,910-56,790,211 RAD51C
    nsv5938607copy number variation1nstd209human GRCh38 chr17: 58,730,429-58,731,510 , GRCh37.p13 chr17: 56,807,790-56,808,871 LOC105371843, RAD51C
    nsv5930112copy number variation1nstd209human GRCh38 chr17: 58,726,454-58,726,607 , GRCh37.p13 chr17: 56,803,815-56,803,968 RAD51C, LOC105371843
    nsv5875771copy number variation1nstd209human GRCh38 chr17: 58,709,537-58,711,180 , GRCh37.p13 chr17: 56,786,898-56,788,541 RAD51C
    nsv5873848copy number variation1nstd209human GRCh38 chr17: 58,730,367-58,731,366 , GRCh37.p13 chr17: 56,807,728-56,808,727 LOC105371843, RAD51C
    nsv5673136copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,798,097-56,801,482 , GRCh38.p12 chr17: 58,720,736-58,724,121 RAD51C, LOC105371843
    nsv5673135copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,780,551-56,787,357 , GRCh38.p12 chr17: 58,703,190-58,709,996 RAD51C
    nsv5673134copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,769,920-56,811,662 , GRCh38.p12 chr17: 58,692,559-58,734,301 RAD51C, LOC105371843
    nsv5655787insertion1nstd207human GRCh38 chr17: 58,726,610-58,726,610 , GRCh37.p13 chr17: 56,803,971-56,803,971 LOC105371843, RAD51C
    nsv5646722insertion1nstd207human GRCh38 chr17: 58,726,417-58,726,417 , GRCh37.p13 chr17: 56,803,778-56,803,778 RAD51C, LOC105371843
    nsv5589042copy number variation1nstd207human GRCh38 chr17: 58,730,461-58,730,911 , GRCh37.p13 chr17: 56,807,822-56,808,272 RAD51C, LOC105371843
    nsv5587280copy number variation1nstd207human GRCh38 chr17: 58,726,454-58,726,607 , GRCh37.p13 chr17: 56,803,815-56,803,968 RAD51C, LOC105371843
    nsv5564313copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,769,986-56,801,482 , GRCh38.p12 chr17: 58,692,625-58,724,121 RAD51C, LOC105371843
    nsv5564159copy number variation1nstd102humanPathogenic GRCh38 chr17: 58,732,482-58,732,545 , GRCh37 chr17: 56,809,843-56,809,906 RAD51C, LOC105371843
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5533164copy number variation1nstd206human GRCh38 chr17: 58,700,463-58,701,660 , GRCh37.p13 chr17: 56,777,824-56,779,021 RAD51C
    nsv5532380copy number variation1nstd206human GRCh38 chr17: 58,730,402-58,731,532 , GRCh37.p13 chr17: 56,807,763-56,808,893 LOC105371843, RAD51C
    nsv5523702copy number variation1nstd206human GRCh38 chr17: 58,730,462-58,730,912 , GRCh37.p13 chr17: 56,807,823-56,808,273 LOC105371843, RAD51C
    nsv5381036copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,432,304-56,811,583 , GRCh38.p12 chr17: 58,354,943-58,734,222 SEPTIN4-AS1, MTMR4, 13 more genes
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