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    Number of Variants: 13

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885017copy number variation1nstd102humanLikely benign GRCh37 chr3: 52,257,338-52,264,976 , GRCh38.p12 chr3: 52,223,322-52,230,960 TWF2, TLR9
    nsv3875047copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483 TWF2, SLMAP, 132 more genes
    nsv3912778copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,498,433-55,348,528 , GRCh38 chr3: 49,461,000-55,314,500 , NCBI36 chr3: 49,473,437-55,323,568 TWF2, SEMA3G, 160 more genes
    nsv4453518copy number variation1nstd102humanPathogenic GRCh37 chr3: 52,195,134-52,869,037 , GRCh38.p12 chr3: 52,161,118-52,835,021 TWF2, SNORD19B, 42 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 TWF2, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 TWF2, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 TWF2, RPL23AP49, 2875 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 TWF2, UQCRC1, 291 more genes
    nsv3917135copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 51,406,905-55,073,516 , GRCh37 chr3: 51,431,865-55,098,476 , GRCh38 chr3: 51,394,434-55,064,449 TWF2, ACY1, 96 more genes
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 TWF2, DNAH1, 62 more genes
    nsv7097206copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,109,903-53,164,416 , GRCh38.p12 chr3: 52,075,887-53,130,400 TWF2, PHF7, 47 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 TWF2, RRP9, 76 more genes
    nsv4728314copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,975,459-52,561,678 , GRCh38.p12 chr3: 51,941,443-52,527,662 TWF2, ABHD14A-ACY1, 32 more genes
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