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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv7047973inversion1nstd229human GRCh38 chr6: 137,616,754-138,122,441 , GRCh37.p13 chr6: 137,937,891-138,443,578 LINC03004, RPSAP42, 8 more genes
    nsv6817153copy number variation1nstd229human GRCh38 chr6: 137,882,053-137,882,120 , GRCh37.p13 chr6: 138,203,190-138,203,257 TNFAIP3
    nsv6814811copy number variation1nstd229human GRCh38 chr6: 137,861,401-137,900,900 , GRCh37.p13 chr6: 138,182,538-138,222,037 TNFAIP3, WAKMAR2
    nsv6811912copy number variation1nstd229human GRCh38 chr6: 137,801,388-140,356,633 , GRCh37.p13 chr6: 138,122,525-140,677,770 TXLNB, LOC100129844, 38 more genes
    nsv6808949copy number variation1nstd229human GRCh38 chr6: 137,685,601-137,900,900 , GRCh37.p13 chr6: 138,006,738-138,222,037 TNFAIP3, WAKMAR2, 2 more genes
    nsv6804186copy number variation1nstd229human GRCh38 chr6: 137,880,492-137,904,713 , GRCh37.p13 chr6: 138,201,629-138,225,850 TNFAIP3
    nsv6618010copy number variation1nstd223human GRCh38 chr6: 137,866,801-137,867,300 , GRCh37.p13 chr6: 138,187,938-138,188,437 TNFAIP3, WAKMAR2
    nsv6615424copy number variation1nstd223human GRCh38 chr6: 137,866,401-137,868,100 , GRCh37.p13 chr6: 138,187,538-138,189,237 TNFAIP3, WAKMAR2
    nsv6314818copy number variation1nstd102humanPathogenic GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193 PBOV1, IFNGR1, 100 more genes
    nsv6312560copy number variation1nstd102humanUncertain significance GRCh37 chr6: 138,201,188-138,202,456 , GRCh38.p12 chr6: 137,880,051-137,881,319 TNFAIP3
    nsv6312142copy number variation2nstd102humanPathogenic GRCh37 chr6: 137,143,759-138,202,456 , GRCh38.p12 chr6: 136,822,621-137,881,319 SLC35D3, LINC03004, 16 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5901279copy number variation1nstd209human GRCh38 chr6: 137,871,408-137,873,734 , GRCh37.p13 chr6: 138,192,545-138,194,871 TNFAIP3
    nsv5900303copy number variation1nstd209human GRCh38 chr6: 137,862,313-137,879,924 , GRCh37.p13 chr6: 138,183,450-138,201,061 , TNFAIP3, 1 more genes
    nsv5844390copy number variation1nstd209human GRCh38 chr6: 137,872,346-137,879,270 , GRCh37.p13 chr6: 138,193,483-138,200,407 TNFAIP3
    nsv5844300copy number variation1nstd209human GRCh38 chr6: 137,871,371-137,873,870 , GRCh37.p13 chr6: 138,192,508-138,195,007 TNFAIP3
    nsv5844299copy number variation1nstd209human GRCh38 chr6: 137,862,464-137,870,270 , GRCh37.p13 chr6: 138,183,601-138,191,407 , WAKMAR2, 1 more genes
    nsv5682943mobile element insertion2nstd211human GRCh38 chr6: 137,868,711-137,868,711 , GRCh37.p13 chr6: 138,189,848-138,189,848 WAKMAR2, TNFAIP3
    nsv5381523copy number variation1nstd102humanPathogenic GRCh37 chr6: 138,125,829-138,244,816 , GRCh38.p12 chr6: 137,804,692-137,923,679 WAKMAR2, TNFAIP3
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