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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
    nsv7137783insertion1nstd232human GRCh37.p13 chr6: 170,574,141-170,574,141 , GRCh38.p12 chr6: 170,265,053-170,265,053 LOC285804
    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
    nsv7098721copy number variation1nstd102humanUncertain significance GRCh37 chr6: 170,151,754-170,599,227 , GRCh38.p12 chr6: 169,751,658-170,290,139 LOC100131532, LOC107986674, 16 more genes
    nsv7056319inversion1nstd229human GRCh38 chr6: 170,141,158-170,327,845 , GRCh37.p13 chr6: 170,456,382-170,636,933 LOC285804, LINC01624, 7 more genes
    nsv7055799inversion1nstd229human GRCh38 chr6: 169,913,682-170,355,724 , GRCh37.p13 chr6: 170,329,974-170,664,812 LOC105378150, LOC107986674, 12 more genes
    nsv7055500inversion1nstd229human GRCh38 chr6: 169,948,590-170,463,253 , GRCh37.p13 chr6: 170,329,974-170,772,341 LOC102724511, LOC105378150, 13 more genes
    nsv7055447inversion1nstd229human GRCh38 chr6: 170,268,249-170,268,313 , GRCh37.p13 chr6: 170,577,337-170,577,401 LOC285804
    nsv7054785inversion1nstd229human GRCh38 chr6: 169,807,778-170,315,940 , GRCh37.p13 chr6: 170,207,874-170,625,028 RPL12P23, LOC107986674, 12 more genes
    nsv7053745inversion1nstd229human GRCh38 chr6: 170,268,429-170,446,986 , GRCh37.p13 chr6: 170,577,517-170,756,074 LOC285804, LINC01624, 4 more genes
    nsv7051910inversion1nstd229human GRCh38 chr6: 170,141,219-170,327,833 , GRCh37.p13 chr6: 170,456,443-170,636,921 FAM120B, RPL12P23, 7 more genes
    nsv7045902inversion1nstd229human GRCh38 chr6: 170,114,334-170,444,387 , GRCh37.p13 chr6: 170,429,558-170,753,475 RPL12P23, LOC154449, 9 more genes
    nsv7039669inversion1nstd229human GRCh38 chr6: 170,260,757-170,287,308 , GRCh37.p13 chr6: 170,569,845-170,596,396 LOC285804, LINC01624, 2 more genes
    nsv6811379copy number variation1nstd229human GRCh38 chr6: 170,226,823-170,560,969 , GRCh37.p13 chr6: 170,536,613-170,870,057 LOC154449, LOC285804, 8 more genes
    nsv6809665copy number variation1nstd229human GRCh38 chr6: 170,118,479-170,385,433 , GRCh37.p13 chr6: 170,433,703-170,694,521 LOC285804, LOC154449, 8 more genes
    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
    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
    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
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