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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5845056copy number variation2nstd209human GRCh38 chr6: 169,732,074-169,733,073 , GRCh37.p13 chr6: 170,132,170-170,133,169 DYNLT2
    nsv5552611insertion1nstd206human GRCh38 chr6: 169,751,830-169,751,844 , GRCh37.p13 chr6: 170,151,926-170,151,940 DYNLT2, ERMARD
    nsv5454180copy number variation1nstd206human GRCh38 chr6: 169,724,336-169,724,394 , GRCh37.p13 chr6: 170,124,432-170,124,490 DYNLT2, PHF10
    nsv5305017copy number variation1nstd204human GRCh38.p13 chr6: 169,740,648-169,741,166 , GRCh37.p13 chr6: 170,140,744-170,141,262 DYNLT2
    nsv4966027copy number variation1nstd200human GRCh38 chr6: 169,180,752-170,050,020 , GRCh37.p13 chr6: 169,580,847-170,365,244 , LOC100131532, 17 more genes
    nsv4818145copy number variation1nstd200human GRCh37 chr6: 170,140,750-170,141,257 , GRCh38.p12 chr6|NT_187552.1: 15,856-16,363 , GRCh38.p12 chr6: 169,740,654-169,741,161 DYNLT2
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4729261copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,580,012-170,919,482 , GRCh38.p12 chr6: 167,166,524-170,610,394 LOC107986549, AFDN, 81 more genes
    nsv4675958copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,440,417-170,919,482 , GRCh38.p12 chr6: 167,026,929-170,610,394 CCR6, HGC6.3, 86 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675577copy number variation1nstd102humanPathogenic GRCh37 chr6: 170,136,337-170,919,482 , GRCh38.p12 chr6: 169,736,241-170,610,394 LOC107986676, LOC105378149, 22 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 more genes
    nsv4615815copy number variation1nstd183human GRCh37 chr6: 170,123,565-170,125,108 , GRCh38.p12 chr6: 169,723,469-169,725,012 PHF10, DYNLT2
    nsv4605154copy number variation1nstd183human GRCh37 chr6: 170,123,914-170,123,959 , GRCh38.p12 chr6: 169,723,818-169,723,863 DYNLT2, PHF10
    nsv4486197mobile element insertion1nstd166human GRCh37.p13 chr6: 170,137,639-170,137,639 , GRCh38.p12 chr6: 169,737,543-169,737,543 , GRCh38.p12 chr6|NT_187552.1: 12,745-12,745 DYNLT2
    nsv4455397copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394 TBP, LOC112267970, 108 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4400464copy number variation1nstd174human GRCh37 chr6: 170,123,196-170,125,574 , GRCh38.p12 chr6: 169,723,100-169,725,478 PHF10, DYNLT2
    nsv4376081copy number variation1nstd173human GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394 , LOC107986550, 151 more genes
    nsv4350147copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,311,806-170,881,789 , GRCh38.p12 chr6: 167,911,126-170,572,701 LINC00574, LOC107986674, 56 more genes
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