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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5501249copy number variation1nstd206human GRCh38 chr13: 47,943,618-47,943,696 , GRCh37.p13 chr13: 48,517,753-48,517,831 SUCLA2
    nsv5356870translocation1nstd200human GRCh38 chr13: 48,000,548-48,000,548 , GRCh38 chr13: 48,000,413-48,000,413 , GRCh37.p13 chr13: 48,574,548-48,574,548 , GRCh37.p13 chr13: 48,574,683-48,574,683 SUCLA2
    nsv5304235copy number variation1nstd204human GRCh37.p13 chr13: 48,379,250-48,587,674 , GRCh38.p13 chr13: 47,805,115-48,013,538 SUCLA2, LINC00562, 1 more genes
    nsv5275897copy number variation1nstd204human GRCh38.p13 chr13: 47,805,101-48,013,500 , GRCh37.p13 chr13: 48,379,236-48,587,636 SUCLA2, LINC00562, 1 more genes
    nsv5271693copy number variation1nstd204human GRCh38.p13 chr13: 47,954,457-47,955,756 , GRCh37.p13 chr13: 48,528,592-48,529,891 SUCLA2
    nsv5269329copy number variation1nstd204human GRCh38.p13 chr13: 47,985,159-47,986,792 , GRCh37.p13 chr13: 48,559,294-48,560,927 SUCLA2
    nsv5261136copy number variation1nstd204human GRCh38.p13 chr13: 47,933,700-48,010,546 , GRCh37.p13 chr13: 48,507,835-48,584,682 SUCLA2, LINC00444
    nsv5155951mobile element insertion1nstd203human GRCh38 chr13: 47,985,610-47,985,623 , GRCh37.p13 chr13: 48,559,745-48,559,758 SUCLA2
    nsv5153968mobile element insertion1nstd203human GRCh38 chr13: 47,997,955-47,997,967 , GRCh37.p13 chr13: 48,572,090-48,572,102 SUCLA2
    nsv5004577copy number variation1nstd200human GRCh38 chr13: 47,997,505-47,997,697 , GRCh37.p13 chr13: 48,571,640-48,571,832 SUCLA2
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4847270copy number variation1nstd200human GRCh37 chr13: 48,379,273-48,587,650 , GRCh38.p12 chr13: 47,805,138-48,013,514 SUCLA2, LINC00444, 1 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4613092copy number variation1nstd183human GRCh37 chr13: 48,562,451-48,563,036 , GRCh38.p12 chr13: 47,988,316-47,988,901 SUCLA2
    nsv4611945copy number variation1nstd183human GRCh37 chr13: 48,562,822-48,563,206 , GRCh38.p12 chr13: 47,988,687-47,989,071 SUCLA2
    nsv4529981copy number variation1nstd166human GRCh37.p13 chr13: 48,540,225-48,540,284 , GRCh38.p12 chr13: 47,966,090-47,966,149 SUCLA2
    nsv4529058copy number variation1nstd166human GRCh37.p13 chr13: 48,551,557-48,559,908 , GRCh38.p12 chr13: 47,977,422-47,985,773 SUCLA2
    nsv4513141mobile element insertion1nstd166human GRCh37.p13 chr13: 48,572,090-48,572,090 , GRCh38.p12 chr13: 47,997,955-47,997,955 SUCLA2
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