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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7047929inversion1nstd229human GRCh38 chr6: 2,249,577-5,332,355 , GRCh37.p13 chr6: 2,249,811-5,332,588 LOC107986561, NQO2-AS1, 67 more genes
    nsv7044205inversion1nstd229human GRCh38 chr6: 2,472,898-4,774,625 , GRCh37.p13 chr6: 2,473,132-4,774,859 TOMM5P1, PXDC1, 56 more genes
    nsv6796560copy number variation1nstd229human GRCh38 chr6: 3,276,395-3,276,420 , GRCh37.p13 chr6: 3,276,629-3,276,654 SLC22A23, PSMG4
    nsv6788767copy number variation1nstd229human GRCh38 chr6: 3,281,767-3,286,762 , GRCh37.p13 chr6: 3,282,001-3,286,996 SLC22A23, PSMG4
    nsv6785298copy number variation1nstd229human GRCh38 chr6: 2,759,301-4,105,800 , GRCh37.p13 chr6: 2,759,535-4,106,034 LOC107986557, SERPINB9-AS1, 39 more genes
    nsv6783745copy number variation1nstd229human GRCh38 chr6: 3,273,113-3,273,194 , GRCh37.p13 chr6: 3,273,347-3,273,428 PSMG4, SLC22A23
    nsv6783039copy number variation1nstd229human GRCh38 chr6: 3,253,224-3,255,274 , GRCh37.p13 chr6: 3,253,458-3,255,508 PSMG4
    nsv6782939copy number variation1nstd229human GRCh38 chr6: 3,288,699-3,292,949 , GRCh37.p13 chr6: 3,288,933-3,293,183 SLC22A23, PSMG4
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6557204inversion1nstd223human GRCh38 chr6: 3,253,560-3,254,826 , GRCh37.p13 chr6: 3,253,794-3,255,060 PSMG4
    nsv6314746copy number variation1nstd102humanPathogenic GRCh37 chr6: 375,263-3,655,142 , GRCh38.p12 chr6: 375,263-3,654,908 RN7SL352P, SERPINB8P1, 55 more genes
    nsv6313679copy number variation1nstd102humanPathogenic GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385 SERPINB9P1, LOC101927691, 59 more genes
    nsv6136505copy number variation1nstd213human GRCh37 chr6: 380,000-11,010,001 , GRCh38.p12 chr6: 380,000-11,009,768 BMP6, BPHL, 178 more genes
    nsv6135513copy number variation1nstd213human GRCh37 chr6: 380,000-10,980,001 , GRCh38.p12 chr6: 380,000-10,979,768 BMP6, BPHL, 178 more genes
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5560290sequence alteration1nstd206human GRCh38 chr6: 3,280,492-3,281,158 , GRCh37.p13 chr6: 3,280,726-3,281,392 SLC22A23, PSMG4
    nsv5455256copy number variation1nstd206human GRCh38 chr6: 3,295,391-3,295,444 , GRCh37.p13 chr6: 3,295,625-3,295,678 SLC22A23, PSMG4
    nsv5454290copy number variation1nstd206human GRCh38 chr6: 3,294,261-3,294,317 , GRCh37.p13 chr6: 3,294,495-3,294,551 PSMG4, SLC22A23
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