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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926338copy number variation1nstd209human GRCh38 chr11: 112,967,650-112,967,832 , GRCh37.p13 chr11: 112,838,372-112,838,554 , GRCh37.p13 chr11|NW_003871078.1: 150,376-150,558 NCAM1
    nsv5922407copy number variation1nstd209human GRCh38 chr11: 113,116,653-113,119,224 , GRCh37.p13 chr11|NW_003871078.1: 299,379-301,950 , GRCh37.p13 chr11: 112,987,375-112,989,946 NCAM1
    nsv5922191copy number variation1nstd209human GRCh38 chr11: 113,185,950-113,188,355 , GRCh37.p13 chr11: 113,056,672-113,059,077 , GRCh37.p13 chr11|NW_003871078.1: 368,676-371,081 NCAM1
    nsv5922129copy number variation1nstd209human GRCh38 chr11: 113,055,989-113,077,603 , GRCh37.p13 chr11: 112,926,711-112,948,325 , GRCh37.p13 chr11|NW_003871078.1: 238,715-260,329 NCAM1
    nsv5909485copy number variation1nstd209human GRCh38 chr11: 113,151,976-113,152,940 , GRCh37.p13 chr11: 113,022,698-113,023,662 , GRCh37.p13 chr11|NW_003871078.1: 334,702-335,666 NCAM1
    nsv5866486copy number variation1nstd209human GRCh38 chr11: 113,055,640-113,076,035 , GRCh37.p13 chr11: 112,926,362-112,946,757 , GRCh37.p13 chr11|NW_003871078.1: 238,366-258,761 NCAM1
    nsv5864300copy number variation1nstd209human GRCh38 chr11: 113,185,938-113,188,386 , GRCh37.p13 chr11: 113,056,660-113,059,108 , GRCh37.p13 chr11|NW_003871078.1: 368,664-371,112 NCAM1
    nsv5854328copy number variation1nstd209human GRCh38 chr11: 113,116,629-113,119,228 , GRCh37.p13 chr11: 112,987,351-112,989,950 , GRCh37.p13 chr11|NW_003871078.1: 299,355-301,954 NCAM1
    nsv5851014copy number variation1nstd209human GRCh38 chr11: 113,073,176-113,074,711 , GRCh37.p13 chr11: 112,943,898-112,945,433 , GRCh37.p13 chr11|NW_003871078.1: 255,902-257,437 NCAM1
    nsv5728400mobile element insertion2nstd211human GRCh38 chr11: 113,197,682-113,197,682 , GRCh37.p13 chr11|NW_003871078.1: 380,408-380,408 , GRCh37.p13 chr11: 113,068,404-113,068,404 NCAM1
    nsv5726602mobile element insertion1nstd211human GRCh38 chr11: 113,271,329-113,271,329 , GRCh37.p13 chr11|NW_003871078.1: 454,055-454,055 , GRCh37.p13 chr11: 113,142,051-113,142,051 NCAM1, NCAM1-AS1
    nsv5561124mobile element insertion1nstd206human GRCh38 chr11: 113,197,682-113,197,733 , GRCh37.p13 chr11|NW_003871078.1: 380,408-380,459 , GRCh37.p13 chr11: 113,068,404-113,068,455 NCAM1
    nsv5513132copy number variation1nstd206human GRCh38 chr11: 113,070,662-113,070,726 , GRCh37.p13 chr11: 112,941,384-112,941,448 , GRCh37.p13 chr11|NW_003871078.1: 253,388-253,452 NCAM1
    nsv5512123copy number variation1nstd206human GRCh38 chr11: 113,000,281-113,003,505 , GRCh37.p13 chr11: 112,871,003-112,874,227 , GRCh37.p13 chr11|NW_003871078.1: 183,007-186,231 NCAM1
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    nsv5508522copy number variation1nstd206human GRCh38 chr11: 113,055,990-113,077,604 , GRCh37.p13 chr11: 112,926,712-112,948,326 , GRCh37.p13 chr11|NW_003871078.1: 238,716-260,330 NCAM1
    nsv5506093copy number variation1nstd206human GRCh38 chr11: 113,151,980-113,152,941 , GRCh37.p13 chr11|NW_003871078.1: 334,706-335,667 , GRCh37.p13 chr11: 113,022,702-113,023,663 NCAM1
    nsv5503858copy number variation1nstd206human GRCh38 chr11: 113,150,438-113,153,593 , GRCh37.p13 chr11: 113,021,160-113,024,315 , GRCh37.p13 chr11|NW_003871078.1: 333,164-336,319 NCAM1
    nsv5501657copy number variation1nstd206human GRCh38 chr11: 112,967,652-112,967,833 , GRCh37.p13 chr11|NW_003871078.1: 150,378-150,559 , GRCh37.p13 chr11: 112,838,374-112,838,555 NCAM1
    nsv5497117copy number variation1nstd206human GRCh38 chr11: 113,091,228-113,091,289 , GRCh37.p13 chr11|NW_003871078.1: 273,954-274,015 , GRCh37.p13 chr11: 112,961,950-112,962,011 NCAM1
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