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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924968copy number variation1nstd209human GRCh38 chr10: 116,106,491-116,106,782 , GRCh37.p13 chr10: 117,866,002-117,866,293 GFRA1
    nsv5919846copy number variation1nstd209human GRCh38 chr10: 116,206,513-116,212,459 , GRCh37.p13 chr10: 117,966,025-117,971,971 GFRA1
    nsv5913758copy number variation1nstd209human GRCh38 chr10: 116,269,993-116,270,143 , GRCh37.p13 chr10: 118,029,505-118,029,655 GFRA1
    nsv5913412copy number variation1nstd209human GRCh38 chr10: 116,135,182-116,138,195 , GRCh37.p13 chr10: 117,894,693-117,897,706 GFRA1
    nsv5910898copy number variation1nstd209human GRCh38 chr10: 116,165,308-116,165,428 , GRCh37.p13 chr10: 117,924,820-117,924,940 GFRA1
    nsv5863075copy number variation1nstd209human GRCh38 chr10: 116,135,157-116,138,156 , GRCh37.p13 chr10: 117,894,668-117,897,667 GFRA1
    nsv5858209copy number variation1nstd209human GRCh38 chr10: 116,206,498-116,212,606 , GRCh37.p13 chr10: 117,966,010-117,972,118 GFRA1
    nsv5726106mobile element insertion1nstd211human GRCh38 chr10: 116,144,146-116,144,146 , GRCh37.p13 chr10: 117,903,657-117,903,657 GFRA1
    nsv5703869mobile element insertion1nstd211human GRCh38 chr10: 116,171,578-116,171,578 , GRCh37.p13 chr10: 117,931,090-117,931,090 GFRA1
    nsv5698522mobile element insertion1nstd211human GRCh38 chr10: 116,062,496-116,062,496 , GRCh37.p13 chr10: 117,822,007-117,822,007 GFRA1
    nsv5637148insertion1nstd207human GRCh38 chr10: 116,117,533-116,117,533 , GRCh37.p13 chr10: 117,877,044-117,877,044 GFRA1
    nsv5629134insertion1nstd207human GRCh38 chr10: 116,064,085-116,064,085 , GRCh37.p13 chr10: 117,823,596-117,823,596 GFRA1
    nsv5625384insertion1nstd207human GRCh38 chr10: 116,148,076-116,148,076 , GRCh37.p13 chr10: 117,907,587-117,907,587 GFRA1
    nsv5601433copy number variation1nstd207human GRCh38 chr10: 116,196,656-116,196,706 , GRCh37.p13 chr10: 117,956,168-117,956,218 GFRA1
    nsv5593058copy number variation1nstd207human GRCh38 chr10: 116,196,560-116,196,670 , GRCh37.p13 chr10: 117,956,072-117,956,182 GFRA1
    nsv5587964copy number variation1nstd207human GRCh38 chr10: 116,165,308-116,165,428 , GRCh37.p13 chr10: 117,924,820-117,924,940 GFRA1
    nsv5586876copy number variation1nstd207human GRCh38 chr10: 116,244,362-116,244,431 , GRCh37.p13 chr10: 118,003,874-118,003,943 GFRA1
    nsv5503025copy number variation1nstd206human GRCh38 chr10: 116,260,700-116,260,802 , GRCh37.p13 chr10: 118,020,212-118,020,314 GFRA1
    nsv5501078copy number variation1nstd206human GRCh38 chr10: 116,165,309-116,165,429 , GRCh37.p13 chr10: 117,924,821-117,924,941 GFRA1
    nsv5498666copy number variation1nstd206human GRCh38 chr10: 116,113,571-116,173,698 , GRCh37.p13 chr10: 117,873,082-117,933,210 GFRA1
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