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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5883533copy number variation2nstd209human GRCh38 chr20: 25,846,325-25,852,190 , GRCh37.p13 chr20: 25,826,961-25,832,826 LOC101926935, BSNDP2
    nsv5882777copy number variation2nstd209human GRCh38 chr20: 25,848,058-25,882,245 , GRCh37.p13 chr20: 25,828,694-25,862,881 LOC101926935
    nsv5667496inversion1nstd207human GRCh37.p13 chr20: 25,825,790-25,991,321 , GRCh38 chr20: 25,845,154-26,010,685 CFTRP1, LOC100134868, 3 more genes
    nsv5598479copy number variation1nstd207human GRCh38 chr20: 25,783,258-25,845,205 , GRCh37.p13 chr20: 25,763,894-25,825,841 FAM182B, BSNDP2, 2 more genes
    nsv5595451copy number variation1nstd207human GRCh38 chr20: 25,845,154-25,845,518 , GRCh37.p13 chr20: 25,825,790-25,826,154 BSNDP2, LOC101926935
    nsv5331834translocation1nstd200human GRCh37 chr20: 25,834,867-25,834,867 , GRCh37 chr7: 57,706,456-57,706,456 , GRCh38.p12 chr20: 25,854,231-25,854,231 , GRCh38.p12 chr7: 57,646,750-57,646,750 LOC101926935
    nsv5328014copy number variation1nstd204human GRCh38.p13 chr20: 25,516,433-25,858,450 , GRCh37.p13 chr20: 25,497,069-25,839,086 LOC107985400, LOC105372582, 12 more genes
    nsv5295140copy number variation1nstd204human GRCh38.p13 chr20: 25,847,715-25,849,468 , GRCh37.p13 chr20: 25,828,351-25,830,104 LOC101926935
    nsv5294024copy number variation1nstd204human GRCh38.p13 chr20: 25,840,301-25,847,200 , GRCh37.p13 chr20: 25,820,937-25,827,836 LOC101926935, BSNDP2
    nsv5293059copy number variation1nstd204human GRCh38.p13 chr20: 25,834,201-25,844,100 , GRCh37.p13 chr20: 25,814,837-25,824,736 BSNDP2, LOC101926935
    nsv5292935copy number variation1nstd204human GRCh38.p13 chr20: 25,802,501-25,844,100 , GRCh37.p13 chr20: 25,783,137-25,824,736 LOC101926935, BSNDP2
    nsv5291061copy number variation1nstd204human GRCh38.p13 chr20: 25,846,301-25,847,200 , GRCh37.p13 chr20: 25,826,937-25,827,836 LOC101926935, BSNDP2
    nsv5287687copy number variation1nstd204human GRCh38.p13 chr20: 25,842,901-25,847,300 , GRCh37.p13 chr20: 25,823,537-25,827,936 LOC101926935, BSNDP2
    nsv5286937copy number variation1nstd204human GRCh38.p13 chr20: 25,845,196-25,852,602 , GRCh37.p13 chr20: 25,825,832-25,833,238 LOC101926935, BSNDP2
    nsv5283621copy number variation1nstd204human GRCh38.p13 chr20: 25,844,301-25,845,200 , GRCh37.p13 chr20: 25,824,937-25,825,836 BSNDP2, LOC101926935
    nsv5280818copy number variation1nstd204human GRCh38.p13 chr20: 25,834,201-25,845,900 , GRCh37.p13 chr20: 25,814,837-25,826,536 LOC101926935, BSNDP2
    nsv5025242copy number variation1nstd200human GRCh38 chr20: 25,516,440-25,858,448 , GRCh37.p13 chr20: 25,497,076-25,839,084 BSNDP1, RN7SL594P, 12 more genes
    nsv4865508copy number variation1nstd200human GRCh37 chr20: 25,497,076-25,839,084 , GRCh38.p12 chr20: 25,516,440-25,858,448 FAM182B, VN1R108P, 12 more genes
    nsv4749508copy number variation1nstd199human GRCh37 chr20: 25,763,845-25,825,792 , GRCh38.p12 chr20: 25,783,209-25,845,156 FAM182B, BSNDP2, 2 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
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