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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3883074copy number variation2nstd102humannot provided, Benign GRCh37 chr3: 151,514,590-151,574,286 , GRCh38 chr3: 151,796,802-151,856,498 AADAC, AADACL2-AS1
    nsv3886508copy number variation1nstd102humanBenign GRCh37 chr3: 151,511,561-151,559,645 , GRCh38.p12 chr3: 151,793,773-151,841,857 AADAC, AADACL2-AS1
    nsv3884728copy number variation1nstd102humanBenign GRCh37 chr3: 151,510,257-151,554,749 , GRCh38.p12 chr3: 151,792,469-151,836,961 AADAC, AADACL2-AS1
    nsv3883117copy number variation2nstd102humannot provided GRCh37 chr3: 151,514,590-151,546,041 , GRCh38 chr3: 151,796,802-151,828,253 AADAC, AADACL2-AS1
    esv3648126copy number variation1estd216humannot provided GRCh37 chr3: 151,514,590-151,574,286 , GRCh38.p12 chr3: 151,796,802-151,856,498 AADAC, AADACL2-AS1, 1 more genes
    esv3648129copy number variation1estd216humannot provided GRCh37 chr3: 151,514,590-151,546,041 , GRCh38.p12 chr3: 151,796,802-151,828,253 AADAC, AADACL2-AS1, 1 more genes
    esv3648128copy number variation1estd216humannot provided GRCh37 chr3: 151,514,590-151,546,041 , GRCh38.p12 chr3: 151,796,802-151,828,253 AADAC, AADACL2-AS1, 1 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 AADAC, LOC102724145, 273 more genes
    nsv3887637copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,425,748-153,220,169 , GRCh38.p12 chr3: 148,707,961-153,502,380 AADAC, LOC101927942, 97 more genes
    nsv4674301copy number variation1nstd102humanPathogenic GRCh37 chr3: 149,404,255-152,786,331 , GRCh38.p12 chr3: 149,686,468-153,068,542 AADAC, EIF3JP2, 63 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 AADAC, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 AADAC, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 AADAC, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 AADAC, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 AADAC, H1-10, 846 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 AADAC, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 AADAC, RNU6-901P, 673 more genes
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 AADAC, LOC105374167, 394 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 AADAC, MBNL1-AS1, 339 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 AADAC, MTAPP1, 339 more genes
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