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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148221copy number variation1nstd102humanPathogenic GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958 RNU6-824P, LOC105378067, 97 more genes
    nsv7145082insertion1nstd232human GRCh37.p13 chr6: 155,626,857-155,626,857 , GRCh38.p12 chr6: 155,305,723-155,305,723 TFB1M
    nsv7057653inversion1nstd229human GRCh38 chr6: 155,088,001-159,627,095 , GRCh37.p13 chr6: 155,409,135-160,048,127 SNORD28B, NMTRV-TAC1-1, 62 more genes
    nsv7053022inversion1nstd229human GRCh38 chr6: 153,431,159-160,785,697 , GRCh37.p13 chr6: 153,752,294-161,206,729 OPRM1, FNDC1-AS1, 106 more genes
    nsv7052273inversion1nstd229human GRCh38 chr6: 153,428,141-160,785,922 , GRCh37.p13 chr6: 153,749,276-161,206,954 LOC442272, CACYBPP3, 106 more genes
    nsv7050008inversion1nstd229human GRCh38 chr6: 153,421,054-160,785,901 , GRCh37.p13 chr6: 153,742,189-161,206,933 SLC22A2, IGF2R, 108 more genes
    nsv7040600inversion1nstd229human GRCh38 chr6: 153,683,778-158,739,378 , GRCh37.p13 chr6: 154,004,913-159,160,410 TMEM242, RPL17P24, 59 more genes
    nsv6816865copy number variation1nstd229human GRCh38 chr6: 155,237,279-155,253,240 , GRCh37.p13 chr6: 155,558,413-155,574,374 TIAM2, TFB1M
    nsv6816812copy number variation1nstd229human GRCh38 chr6: 155,264,756-155,269,564 , GRCh37.p13 chr6: 155,585,890-155,590,698 CLDN20, TFB1M
    nsv6815648copy number variation1nstd229human GRCh38 chr6: 155,250,930-155,255,477 , GRCh37.p13 chr6: 155,572,064-155,576,611 TFB1M, TIAM2
    nsv6811703copy number variation1nstd229human GRCh38 chr6: 155,267,584-155,271,287 , GRCh37.p13 chr6: 155,588,718-155,592,421 TFB1M, CLDN20
    nsv6811394copy number variation1nstd229human GRCh38 chr6: 155,269,849-155,270,868 , GRCh37.p13 chr6: 155,590,983-155,592,002 CLDN20, TFB1M
    nsv6807808copy number variation1nstd229human GRCh38 chr6: 155,229,991-155,250,902 , GRCh37.p13 chr6: 155,551,125-155,572,036 TFB1M, TIAM2
    nsv6806235copy number variation1nstd229human GRCh38 chr6: 155,246,663-155,246,716 , GRCh37.p13 chr6: 155,567,797-155,567,850 TIAM2, TFB1M
    nsv6806193copy number variation1nstd229human GRCh38 chr6: 155,301,756-155,305,005 , GRCh37.p13 chr6: 155,622,890-155,626,139 TFB1M
    nsv6805175copy number variation1nstd229human GRCh38 chr6: 155,290,418-155,290,541 , GRCh37.p13 chr6: 155,611,552-155,611,675 TFB1M
    nsv6804362copy number variation1nstd229human GRCh38 chr6: 155,300,053-155,313,072 , GRCh37.p13 chr6: 155,621,187-155,634,206 TFB1M
    nsv6801733copy number variation1nstd229human GRCh38 chr6: 155,257,385-155,278,111 , GRCh37.p13 chr6: 155,578,519-155,599,245 CLDN20, TFB1M, 1 more genes
    nsv6798189copy number variation1nstd229human GRCh38 chr6: 154,294,974-156,930,933 , GRCh37.p13 chr6: 154,616,108-157,252,067 LOC105378073, LOC105378067, 28 more genes
    nsv6606752copy number variation1nstd223human GRCh38 chr6: 155,267,584-155,271,284 , GRCh37.p13 chr6: 155,588,718-155,592,418 CLDN20, TFB1M
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