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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973076insertion1nstd209human GRCh38 chr14: 85,631,112-85,631,112 , GRCh37.p13 chr14: 86,097,456-86,097,456 FLRT2
    nsv5972626insertion1nstd209human GRCh38 chr14: 85,615,721-85,615,721 , GRCh37.p13 chr14: 86,082,065-86,082,065 FLRT2
    nsv5971683insertion1nstd209human GRCh38 chr14: 85,643,354-85,643,354 , GRCh37.p13 chr14: 86,109,698-86,109,698 FLRT2
    nsv5941767copy number variation1nstd209human GRCh38 chr14: 85,584,707-85,584,914 , GRCh37.p13 chr14: 86,051,051-86,051,258 FLRT2
    nsv5932726copy number variation1nstd209human GRCh38 chr14: 85,645,940-85,646,082 , GRCh37.p13 chr14: 86,112,284-86,112,426 FLRT2
    nsv5931205copy number variation1nstd209human GRCh38 chr14: 85,598,657-85,599,384 , GRCh37.p13 chr14: 86,065,001-86,065,728 FLRT2
    nsv5854780copy number variation1nstd209human GRCh38 chr14: 85,551,019-85,552,273 , GRCh37.p13 chr14: 86,017,363-86,018,617 FLRT2
    nsv5721019mobile element insertion1nstd211human GRCh38 chr14: 85,633,029-85,633,029 , GRCh37.p13 chr14: 86,099,373-86,099,373 FLRT2
    nsv5703933mobile element insertion2nstd211human GRCh38 chr14: 85,536,753-85,536,753 , GRCh37.p13 chr14: 86,003,097-86,003,097 FLRT2
    nsv5653719insertion1nstd207human GRCh38 chr14: 85,615,721-85,615,721 , GRCh37.p13 chr14: 86,082,065-86,082,065 FLRT2
    nsv5651799insertion1nstd207human GRCh38 chr14: 85,643,354-85,643,354 , GRCh37.p13 chr14: 86,109,698-86,109,698 FLRT2
    nsv5543062insertion1nstd206human GRCh38 chr14: 85,615,721-85,615,721 , GRCh37.p13 chr14: 86,082,065-86,082,065 FLRT2
    nsv5537568insertion1nstd206human GRCh38 chr14: 85,631,122-85,631,163 , GRCh37.p13 chr14: 86,097,466-86,097,507 FLRT2
    nsv5511217copy number variation1nstd206human GRCh38 chr14: 85,546,019-85,546,106 , GRCh37.p13 chr14: 86,012,363-86,012,450 FLRT2
    nsv5504231copy number variation1nstd206human GRCh38 chr14: 85,598,660-85,599,385 , GRCh37.p13 chr14: 86,065,004-86,065,729 FLRT2
    nsv5500543copy number variation1nstd206human GRCh38 chr14: 85,608,458-85,639,161 , GRCh37.p13 chr14: 86,074,802-86,105,505 FLRT2
    nsv5499683copy number variation1nstd206human GRCh38 chr14: 85,606,766-85,606,826 , GRCh37.p13 chr14: 86,073,110-86,073,170 FLRT2
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5495031copy number variation1nstd206human GRCh38 chr14: 85,645,943-85,646,083 , GRCh37.p13 chr14: 86,112,287-86,112,427 FLRT2
    nsv5416395mobile element insertion1nstd206human GRCh38 chr14: 85,536,753-85,536,804 , GRCh37.p13 chr14: 86,003,097-86,003,148 FLRT2
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