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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5639218insertion1nstd207human GRCh38 chr5: 71,387,884-71,387,884 , GRCh37.p13 chr5: 70,683,711-70,683,711 LINC02197
    nsv5634154insertion1nstd207human GRCh38 chr5: 71,345,075-71,345,075 , GRCh37.p13 chr5: 70,640,902-70,640,902 , LINC02197, 1 more genes
    nsv5631685insertion1nstd207human GRCh38 chr5: 71,424,947-71,424,947 , GRCh37.p13 chr5: 70,720,774-70,720,774 LINC02197
    nsv5624598insertion1nstd207human GRCh38 chr5: 71,416,819-71,416,819 , GRCh37.p13 chr5: 70,712,646-70,712,646 LINC02197
    nsv5574321copy number variation1nstd207human GRCh38 chr5: 71,337,157-71,337,233 , GRCh37.p13 chr5: 70,632,984-70,633,060 , LINC02197, 1 more genes
    nsv5572986copy number variation1nstd207human GRCh38 chr5: 71,437,311-71,437,368 , GRCh37.p13 chr5: 70,733,138-70,733,195 LINC02197
    nsv5568320copy number variation1nstd207human GRCh38 chr5: 71,340,128-71,340,442 , GRCh37.p13 chr5: 70,635,955-70,636,269 , LINC02197, 1 more genes
    nsv5565207copy number variation1nstd207human GRCh38 chr5: 71,345,176-71,345,865 , GRCh37.p13 chr5: 70,641,003-70,641,692 , LINC02197, 1 more genes
    nsv5468709copy number variation1nstd206human GRCh38 chr5: 71,324,879-71,326,352 , GRCh37.p13 chr5: 70,620,706-70,622,179 , LINC02197
    nsv5467486copy number variation1nstd206human GRCh38 chr5: 71,382,663-71,383,084 , GRCh37.p13 chr5: 70,678,490-70,678,911 PMCHL2, LINC02197
    nsv5462736copy number variation1nstd206human GRCh38 chr5: 71,393,971-71,402,217 , GRCh37.p13 chr5: 70,689,798-70,698,044 LINC02197
    nsv5362316translocation1nstd200human GRCh38 chr5: 71,382,663-71,382,663 , GRCh38 chr5: 71,383,084-71,383,084 , GRCh37.p13 chr5: 70,678,490-70,678,490 , GRCh37.p13 chr5: 70,678,911-70,678,911 LINC02197, PMCHL2
    nsv5240032copy number variation1nstd204human GRCh38.p13 chr5: 71,344,301-71,354,200 , GRCh37.p13 chr5: 70,640,128-70,650,027 , LINC02197, 1 more genes
    nsv5239679copy number variation1nstd204human GRCh38.p13 chr5: 71,332,401-71,343,500 , GRCh37.p13 chr5: 70,628,228-70,639,327 , LINC02197, 1 more genes
    nsv5238863copy number variation1nstd204human GRCh38.p13 chr5: 71,349,301-71,350,200 , GRCh37.p13 chr5: 70,645,128-70,646,027 , LINC02197
    nsv5236782copy number variation1nstd204human GRCh38.p13 chr5: 71,401,697-71,403,111 , GRCh37.p13 chr5: 70,697,524-70,698,938 LINC02197
    nsv5235291copy number variation1nstd204human GRCh38.p13 chr5: 71,395,079-71,396,081 , GRCh37.p13 chr5: 70,690,906-70,691,908 LINC02197
    nsv5234880copy number variation1nstd204human GRCh38.p13 chr5: 71,340,601-71,353,500 , GRCh37.p13 chr5: 70,636,428-70,649,327 , LINC02197, 1 more genes
    nsv5234422copy number variation1nstd204human GRCh38.p13 chr5: 71,324,301-71,330,100 , GRCh37.p13 chr5: 70,620,128-70,625,927 , LINC02197
    nsv5232847copy number variation1nstd204human GRCh38.p13 chr5: 71,338,101-71,341,800 , GRCh37.p13 chr5: 70,633,928-70,637,627 , LINC02197, 1 more genes
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