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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971756inversion1nstd209human GRCh38 chr3: 177,669,105-179,519,336 , GRCh37.p13 chr3: 177,386,893-179,237,124 , PIK3CA, 24 more genes
    nsv5966541insertion1nstd209human GRCh38 chr3: 178,817,218-178,817,218 , GRCh37.p13 chr3: 178,535,006-178,535,006 KCNMB2-AS1, KCNMB2
    nsv5964532insertion1nstd209human GRCh38 chr3: 178,757,840-178,757,840 , GRCh37.p13 chr3: 178,475,628-178,475,628 KCNMB2, KCNMB2-AS1
    nsv5907482copy number variation1nstd209human GRCh38 chr3: 178,621,366-178,621,418 , GRCh37.p13 chr3: 178,339,154-178,339,206 KCNMB2, KCNMB2-AS1
    nsv5907384copy number variation1nstd209human GRCh38 chr3: 178,686,850-178,687,579 , GRCh37.p13 chr3: 178,404,638-178,405,367 KCNMB2, KCNMB2-AS1
    nsv5905177copy number variation1nstd209human GRCh38 chr3: 178,570,448-178,579,162 , GRCh37.p13 chr3: 178,288,236-178,296,950 KCNMB2-AS1, KCNMB2
    nsv5898120copy number variation1nstd209human GRCh38 chr3: 178,760,349-178,760,444 , GRCh37.p13 chr3: 178,478,137-178,478,232 KCNMB2-AS1, KCNMB2
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5896099copy number variation1nstd209human GRCh38 chr3: 178,809,233-178,809,553 , GRCh37.p13 chr3: 178,527,021-178,527,341 KCNMB2, KCNMB2-AS1
    nsv5895620copy number variation1nstd209human GRCh38 chr3: 178,832,342-178,833,082 , GRCh37.p13 chr3: 178,550,130-178,550,870 KCNMB2, KCNMB2-AS1
    nsv5893841copy number variation1nstd209human GRCh38 chr3: 178,757,995-178,758,059 , GRCh37.p13 chr3: 178,475,783-178,475,847 KCNMB2, KCNMB2-AS1
    nsv5892103copy number variation1nstd209human GRCh38 chr3: 178,757,741-178,758,164 , GRCh37.p13 chr3: 178,475,529-178,475,952 KCNMB2, KCNMB2-AS1
    nsv5892082copy number variation1nstd209human GRCh38 chr3: 178,759,330-178,759,387 , GRCh37.p13 chr3: 178,477,118-178,477,175 KCNMB2-AS1, KCNMB2
    nsv5889225copy number variation1nstd209human GRCh38 chr3: 178,758,160-178,759,316 , GRCh37.p13 chr3: 178,475,948-178,477,104 KCNMB2-AS1, KCNMB2
    nsv5888740copy number variation1nstd209human GRCh38 chr3: 178,758,363-178,758,414 , GRCh37.p13 chr3: 178,476,151-178,476,202 KCNMB2-AS1, KCNMB2
    nsv5888517copy number variation1nstd209human GRCh38 chr3: 178,654,942-178,654,996 , GRCh37.p13 chr3: 178,372,730-178,372,784 KCNMB2-AS1, KCNMB2
    nsv5725833mobile element insertion2nstd211human GRCh38 chr3: 178,777,298-178,777,298 , GRCh37.p13 chr3: 178,495,086-178,495,086 KCNMB2-AS1, KCNMB2
    nsv5690893mobile element insertion2nstd211human GRCh38 chr3: 178,673,038-178,673,038 , GRCh37.p13 chr3: 178,390,826-178,390,826 KCNMB2, KCNMB2-AS1
    nsv5690726mobile element insertion1nstd211human GRCh38 chr3: 178,545,814-178,545,814 , GRCh37.p13 chr3: 178,263,602-178,263,602 KCNMB2, KCNMB2-AS1
    nsv5689193mobile element insertion1nstd211human GRCh38 chr3: 178,554,326-178,554,326 , GRCh37.p13 chr3: 178,272,114-178,272,114 KCNMB2, KCNMB2-AS1
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