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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7051730inversion1nstd229human GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278 WDR27, KIF25, 49 more genes
    nsv6801781copy number variation1nstd229human GRCh38 chr6: 169,528,226-169,975,529 , GRCh37.p13 chr6: 169,928,322-170,279,972 LINC00242, LINC00574, 9 more genes
    nsv6798532copy number variation1nstd229human GRCh38 chr6: 169,713,503-169,714,024 , GRCh37.p13 chr6: 170,113,599-170,114,120 PHF10
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634382copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,552,894-170,919,482 , GRCh38.p12 chr6: 168,152,214-170,610,394 LOC101929460, LINC01624, 49 more genes
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6616598copy number variation1nstd223human GRCh38 chr6: 169,539,601-169,704,000 , GRCh37.p13 chr6: 169,939,697-170,104,096 C6orf120, PHF10, 1 more genes
    nsv6615772copy number variation1nstd223human GRCh38 chr6: 169,546,601-170,309,800 , GRCh37.p13 chr6: 169,946,697-170,618,888 ERMARD, C6orf120, 19 more genes
    nsv6613118copy number variation1nstd223human GRCh38 chr6: 169,722,001-169,725,900 , GRCh37.p13 chr6: 170,122,097-170,125,996 PHF10, DYNLT2
    nsv6608026copy number variation1nstd223human GRCh38 chr6: 169,180,752-170,050,020 , GRCh37.p13 chr6: 169,580,847-170,365,244 DYNLT2, LOC107986675, 16 more genes
    nsv6604292copy number variation1nstd223human GRCh38 chr6: 169,644,101-169,762,500 , GRCh37.p13 chr6: 170,044,197-170,162,596 WDR27, C6orf120, 3 more genes
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6315422copy number variation1nstd102humanPathogenic GRCh37 chr6: 168,643,852-170,919,482 , GRCh38.p12 chr6: 168,243,172-170,610,394 LOC105378157, LOC105378140, 48 more genes
    nsv6315394copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,770,398-170,919,482 , GRCh38.p12 chr6: 167,356,910-170,610,394 LINC02544, LOC107986676, 72 more genes
    nsv6313815copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,317,903-170,919,482 , GRCh38.p12 chr6: 166,904,415-170,610,394 LOC285804, LOC105378149, 91 more genes
    nsv6313793copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,212,864-170,919,482 , GRCh38.p12 chr6: 161,791,832-170,610,394 LOC645468, GPR31, 148 more genes
    nsv6313745copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,290,087-170,919,482 , GRCh38.p12 chr6: 162,869,055-170,610,394 HGC6.3, LOC112267970, 143 more genes
    nsv6313560copy number variation1nstd102humanPathogenic GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394 LOC105378142, LOC100289495, 159 more genes
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