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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888878copy number variation1nstd209human GRCh38 chr5: 150,261,102-150,261,170 , GRCh37.p13 chr5: 149,640,665-149,640,733 CAMK2A
    nsv5716905mobile element insertion1nstd211human GRCh38 chr5: 150,249,119-150,249,119 , GRCh37.p13 chr5: 149,628,682-149,628,682 CAMK2A
    nsv5638185insertion1nstd207human GRCh38 chr5: 150,284,573-150,284,573 , GRCh37.p13 chr5: 149,664,136-149,664,136 CAMK2A
    nsv5624591insertion1nstd207human GRCh38 chr5: 150,221,821-150,221,821 , GRCh37.p13 chr5: 149,601,384-149,601,384 CAMK2A
    nsv5565548copy number variation1nstd207human GRCh38 chr5: 150,261,102-150,261,170 , GRCh37.p13 chr5: 149,640,665-149,640,733 CAMK2A
    nsv5468555copy number variation1nstd206human GRCh38 chr5: 150,261,102-150,261,171 , GRCh37.p13 chr5: 149,640,665-149,640,734 CAMK2A
    nsv5386230copy number variation1nstd186human GRCh37 chr5: 149,640,665-149,640,734 , GRCh38.p12 chr5: 150,261,102-150,261,171 CAMK2A
    nsv5362535translocation1nstd200human GRCh38 chr5: 150,243,700-150,243,700 , GRCh38 chr5: 150,243,629-150,243,629 , GRCh37.p13 chr5: 149,623,263-149,623,263 , GRCh37.p13 chr5: 149,623,192-149,623,192 CAMK2A
    nsv5343109translocation1nstd200human GRCh37 chr5: 149,623,192-149,623,192 , GRCh37 chr5: 149,623,263-149,623,263 , GRCh38.p12 chr5: 150,243,629-150,243,629 , GRCh38.p12 chr5: 150,243,700-150,243,700 CAMK2A
    nsv5330651translocation1nstd200human GRCh37 chr5: 149,640,734-149,640,734 , GRCh37 chr5: 149,640,665-149,640,665 , GRCh38.p12 chr5: 150,261,171-150,261,171 , GRCh38.p12 chr5: 150,261,102-150,261,102 CAMK2A
    nsv5305427copy number variation1nstd204human GRCh38.p13 chr5: 150,261,102-150,261,171 , GRCh37.p13 chr5: 149,640,665-149,640,734 CAMK2A
    nsv5097855mobile element insertion1nstd203human GRCh38 chr5: 150,240,292-150,240,305 , GRCh37.p13 chr5: 149,619,855-149,619,868 CAMK2A
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4939165copy number variation1nstd200human GRCh38 chr5: 150,283,430-150,284,026 , GRCh37.p13 chr5: 149,662,993-149,663,589 CAMK2A
    nsv4939164copy number variation1nstd200human GRCh38 chr5: 150,261,102-150,261,171 , GRCh37.p13 chr5: 149,640,665-149,640,734 CAMK2A
    nsv4939163copy number variation1nstd200human GRCh38 chr5: 150,232,598-150,232,675 , GRCh37.p13 chr5: 149,612,161-149,612,238 CAMK2A
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4814946copy number variation1nstd200human GRCh37 chr5: 149,662,993-149,663,589 , GRCh38.p12 chr5: 150,283,430-150,284,026 CAMK2A
    nsv4814945copy number variation1nstd200human GRCh37 chr5: 149,612,161-149,612,238 , GRCh38.p12 chr5: 150,232,598-150,232,675 CAMK2A
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