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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141023copy number variation1nstd232human GRCh38.p12 chr6: 44,253,376-44,253,485 , GRCh37.p13 chr6: 44,221,113-44,221,222 HSP90AB1, SLC35B2, 1 more genes
    nsv6788779copy number variation1nstd229human GRCh38 chr6: 44,217,191-44,323,601 , GRCh37.p13 chr6: 44,184,928-44,291,338 TMEM151B, TCTE1, 7 more genes
    nsv6787193copy number variation1nstd229human GRCh38 chr6: 44,181,401-44,326,600 , GRCh37.p13 chr6: 44,149,138-44,294,337 TMEM151B, AARS2, 10 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv6135515copy number variation1nstd213human GRCh37 chr6: 43,220,000-44,970,001 , GRCh38.p12 chr6: 43,252,262-45,002,264 SLC29A1, NFKBIE, 54 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5343792translocation1nstd200human GRCh37 chr6: 44,221,056-44,221,056 , GRCh37 chr20: 62,460,751-62,460,751 , GRCh38.p12 chr20: 63,829,398-63,829,398 , GRCh38.p12 chr6: 44,253,319-44,253,319 HSP90AB1, ZBTB46, 2 more genes
    nsv4816218copy number variation1nstd200human GRCh37 chr6: 44,224,760-44,225,113 , GRCh38.p12 chr6: 44,257,023-44,257,376 NFKBIE, SLC35B2
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4147253copy number variation1nstd166human GRCh37.p13 chr6: 44,221,118-44,221,223 , GRCh38.p12 chr6: 44,253,381-44,253,486 HSP90AB1, SLC35B2, 1 more genes
    nsv3955959copy number variation1nstd168human GRCh38 chr6: 44,256,360-44,310,256 , GRCh37.p13 chr6: 44,224,097-44,277,993 SLC35B2, TMEM151B, 3 more genes
    nsv3924318copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,336,296-44,558,281 , NCBI36 chr6: 42,444,274-44,666,259 , GRCh38 chr6: 42,368,558-44,590,544 MIR4642, SRF, 82 more genes
    nsv3919521copy number variation1nstd102humanPathogenic NCBI36 chr6: 37,853,123-45,729,558 , GRCh37 chr6: 37,745,145-45,621,580 , GRCh38 chr6: 37,777,369-45,653,843 RPL23P6, LOC102723789, 184 more genes
    nsv3919402copy number variation1nstd102humanPathogenic NCBI36 chr6: 42,769,519-46,417,784 , GRCh37.p13 chr6: 42,661,541-46,309,825 , GRCh38.p12 chr6: 42,693,803-46,342,088 LOC101929770, MRPS18A, 94 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3913481copy number variation1nstd102humanLikely benign NCBI36 chr6: 43,732,603-44,458,145 , GRCh38 chr6: 43,656,888-44,382,430 , GRCh37 chr6: 43,624,625-44,350,167 LOC105375072, EXOSC8P1, 26 more genes
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