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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095480copy number variation4nstd102humanUncertain significance GRCh37 chr19: 39,904,727-42,931,301 , GRCh38.p12 chr19: 39,414,087-42,427,149 CYP2B6, EID2B, 140 more genes
    nsv7076995inversion1nstd229human GRCh38 chr19: 40,814,612-41,132,228 , GRCh37.p13 chr19: 41,320,517-41,638,133 CYP2A6, CYP2A13, 8 more genes
    nsv7073298inversion1nstd229human GRCh38 chr19: 40,825,689-41,122,590 , GRCh37.p13 chr19: 41,331,594-41,628,495 CYP2B6, CYP2G1P, 8 more genes
    nsv7073106inversion1nstd229human GRCh38 chr19: 40,818,178-41,128,674 , GRCh37.p13 chr19: 41,324,083-41,634,579 CYP2A7P1, CYP2A13, 8 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068537inversion1nstd229human GRCh38 chr19: 40,823,692-41,122,636 , GRCh37.p13 chr19: 41,329,597-41,628,541 CYP2F2P, CYP2A7, 8 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7067382inversion1nstd229human GRCh38 chr19: 40,814,816-41,132,017 , GRCh37.p13 chr19: 41,320,721-41,637,922 CYP2B7P, CYP2A13, 8 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7016865copy number variation1nstd229human GRCh38 chr19: 40,830,601-40,864,300 , GRCh37.p13 chr19: 41,336,506-41,370,205 CYP2A6
    nsv7016665copy number variation1nstd229human GRCh38 chr19: 40,833,001-40,864,700 , GRCh37.p13 chr19: 41,338,906-41,370,605 CYP2A6
    nsv7016419copy number variation1nstd229human GRCh38 chr19: 40,831,401-40,865,000 , GRCh37.p13 chr19: 41,337,306-41,370,905 CYP2A6
    nsv7016401copy number variation1nstd229human GRCh38 chr19: 40,842,101-40,875,500 , GRCh37.p13 chr19: 41,348,006-41,381,405 CYP2A6, CYP2A7
    nsv7015751copy number variation1nstd229human GRCh38 chr19: 40,848,301-40,881,900 , GRCh37.p13 chr19: 41,354,206-41,387,805 CYP2A7, CYP2A6
    nsv7015283copy number variation1nstd229human GRCh38 chr19: 40,832,401-40,864,500 , GRCh37.p13 chr19: 41,338,306-41,370,405 CYP2A6
    nsv7012604copy number variation1nstd229human GRCh38 chr19: 40,839,201-40,881,600 , GRCh37.p13 chr19: 41,345,106-41,387,505 CYP2A7, CYP2A6
    nsv7012253copy number variation1nstd229human GRCh38 chr19: 40,833,801-40,875,000 , GRCh37.p13 chr19: 41,339,706-41,380,905 CYP2A6, CYP2A7
    nsv7011361copy number variation1nstd229human GRCh38 chr19: 40,838,801-40,881,600 , GRCh37.p13 chr19: 41,344,706-41,387,505 CYP2A7, CYP2A6
    nsv7011186copy number variation1nstd229human GRCh38 chr19: 40,842,701-40,885,300 , GRCh37.p13 chr19: 41,348,606-41,391,205 CYP2A6, CYP2A7
    nsv7010735copy number variation1nstd229human GRCh38 chr19: 40,848,901-40,885,500 , GRCh37.p13 chr19: 41,354,806-41,391,405 CYP2A7, CYP2A6
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