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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122142copy number variation1nstd186human GRCh37 chr13: 46,719,762-46,720,077 , GRCh38.p12 chr13: 46,145,627-46,145,942 LCP1
    nsv5940592copy number variation1nstd209human GRCh38 chr13: 46,145,627-46,145,952 , GRCh37.p13 chr13: 46,719,762-46,720,087 LCP1
    nsv5697716mobile element insertion1nstd211human GRCh38 chr13: 46,176,179-46,176,179 , GRCh37.p13 chr13: 46,750,314-46,750,314 LCP1
    nsv5588295copy number variation1nstd207human GRCh38 chr13: 46,145,616-46,145,941 , GRCh37.p13 chr13: 46,719,751-46,720,076 LCP1
    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
    nsv5509403copy number variation1nstd206human GRCh38 chr13: 46,162,987-46,163,055 , GRCh37.p13 chr13: 46,737,122-46,737,190 LCP1
    nsv5496910copy number variation1nstd206human GRCh38 chr13: 46,145,627-46,145,942 , GRCh37.p13 chr13: 46,719,762-46,720,077 LCP1
    nsv5495655copy number variation1nstd206human GRCh38 chr13: 46,052,372-46,294,537 , GRCh37.p13 chr13: 46,626,507-46,868,672 LCP1, LOC107984578, 10 more genes
    nsv5418325mobile element insertion1nstd206human GRCh38 chr13: 46,176,179-46,176,230 , GRCh37.p13 chr13: 46,750,314-46,750,365 LCP1
    nsv5385019mobile element deletion2nstd186human GRCh37 chr13: 46,719,762-46,720,077 , GRCh38.p12 chr13: 46,145,627-46,145,942 LCP1
    nsv5315524copy number variation1nstd204human GRCh38.p13 chr13: 46,158,092-46,162,340 , GRCh37.p13 chr13: 46,732,227-46,736,475 LCP1
    nsv5264452copy number variation1nstd204human GRCh38.p13 chr13: 46,157,939-46,162,428 , GRCh37.p13 chr13: 46,732,074-46,736,563 LCP1
    nsv5217207mobile element deletion1nstd204human GRCh38.p13 chr13: 46,145,627-46,145,942 , GRCh37.p13 chr13: 46,719,762-46,720,077 LCP1
    nsv5149705mobile element insertion1nstd203human GRCh38 chr13: 46,176,172-46,176,179 , GRCh37.p13 chr13: 46,750,307-46,750,314 LCP1
    nsv4997314copy number variation1nstd200human GRCh38 chr13: 46,178,285-46,178,569 , GRCh37.p13 chr13: 46,752,420-46,752,704 LCP1
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4899881mobile element deletion1nstd200human GRCh38 chr13: 46,145,627-46,145,942 , GRCh37.p13 chr13: 46,719,762-46,720,077 LCP1
    nsv4832143copy number variation1nstd200human GRCh37 chr13: 46,732,233-46,736,472 , GRCh38.p12 chr13: 46,158,098-46,162,337 LCP1
    nsv4775234mobile element deletion1nstd200human GRCh37 chr13: 46,719,762-46,720,077 , GRCh38.p12 chr13: 46,145,627-46,145,942 LCP1
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