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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897782copy number variation1nstd209human GRCh38 chr3: 19,926,603-19,926,902 , GRCh37.p13 chr3: 19,968,095-19,968,394 EFHB
    nsv5896717copy number variation1nstd209human GRCh38 chr3: 19,936,153-19,936,363 , GRCh37.p13 chr3: 19,977,645-19,977,855 EFHB
    nsv5693970mobile element insertion1nstd211human GRCh38 chr3: 19,913,616-19,913,616 , GRCh37.p13 chr3: 19,955,108-19,955,108 EFHB
    nsv5441793copy number variation1nstd206human GRCh38 chr3: 19,926,795-19,941,010 , GRCh37.p13 chr3: 19,968,287-19,982,502 EFHB, HSPA8P18
    nsv5440012copy number variation1nstd206human GRCh38 chr3: 19,936,155-19,936,364 , GRCh37.p13 chr3: 19,977,647-19,977,856 EFHB
    nsv5439058copy number variation1nstd206human GRCh38 chr3: 19,284,425-19,940,087 , GRCh37.p13 chr3: 19,325,917-19,981,579 KCNH8, EFHB, 4 more genes
    nsv5435622copy number variation1nstd206human GRCh38 chr3: 19,905,657-19,910,821 , GRCh37.p13 chr3: 19,947,149-19,952,313 EFHB
    nsv5404543mobile element insertion1nstd206human GRCh38 chr3: 19,913,616-19,913,667 , GRCh37.p13 chr3: 19,955,108-19,955,159 EFHB
    nsv5377380translocation1nstd200human GRCh38 chr3: 19,926,790-19,926,790 , GRCh38 chr3: 19,928,868-19,928,868 , GRCh37.p13 chr3: 19,970,360-19,970,360 , GRCh37.p13 chr3: 19,968,282-19,968,282 EFHB
    nsv5305866copy number variation1nstd204human GRCh38.p13 chr3: 19,921,828-19,925,654 , GRCh37.p13 chr3: 19,963,320-19,967,146 EFHB
    nsv5216884copy number variation1nstd204human GRCh38.p13 chr3: 19,921,801-19,925,600 , GRCh37.p13 chr3: 19,963,293-19,967,092 EFHB
    nsv5213189copy number variation1nstd204human GRCh38.p13 chr3: 19,921,767-19,925,666 , GRCh37.p13 chr3: 19,963,259-19,967,158 EFHB
    nsv5078668mobile element insertion1nstd203human GRCh38 chr3: 19,907,327-19,907,340 , GRCh37.p13 chr3: 19,948,819-19,948,832 EFHB
    nsv5077880mobile element insertion1nstd203human GRCh38 chr3: 19,914,761-19,914,775 , GRCh37.p13 chr3: 19,956,253-19,956,267 EFHB
    nsv5069577mobile element insertion1nstd203human GRCh38 chr3: 19,932,870-19,932,887 , GRCh37.p13 chr3: 19,974,362-19,974,379 EFHB
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924223copy number variation1nstd200human GRCh38 chr3: 18,945,676-19,948,949 , GRCh37.p13 chr3: 18,987,168-19,990,441 HSPA8P18, EFHB, 9 more genes
    nsv4918100copy number variation1nstd200human GRCh38 chr3: 19,915,741-19,927,831 , GRCh37.p13 chr3: 19,957,233-19,969,323 EFHB
    nsv4918099copy number variation1nstd200human GRCh38 chr3: 19,915,746-19,916,310 , GRCh37.p13 chr3: 19,957,238-19,957,802 EFHB
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