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Items: 1 to 20 of 251

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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
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv6815178copy number variation1nstd229human GRCh38 chr6: 165,272,501-165,279,300 , GRCh37.p13 chr6: 165,685,990-165,692,789 C6orf118
    nsv6811763copy number variation1nstd229human GRCh38 chr6: 165,279,754-165,286,108 , GRCh37.p13 chr6: 165,693,243-165,699,597 C6orf118
    nsv6809710copy number variation1nstd229human GRCh38 chr6: 165,275,149-165,282,445 , GRCh37.p13 chr6: 165,688,638-165,695,934 C6orf118
    nsv6809587copy number variation1nstd229human GRCh38 chr6: 165,302,195-165,302,279 , GRCh37.p13 chr6: 165,715,684-165,715,768 C6orf118
    nsv6805333copy number variation1nstd229human GRCh38 chr6: 165,076,421-165,387,153 , GRCh37.p13 chr6: 165,489,910-165,800,642 C6orf118, LOC105378113, 1 more genes
    nsv6803166copy number variation1nstd229human GRCh38 chr6: 165,307,201-165,319,300 , GRCh37.p13 chr6: 165,720,690-165,732,789 LOC105378113, C6orf118
    nsv6800136copy number variation1nstd229human GRCh38 chr6: 165,286,134-165,290,391 , GRCh37.p13 chr6: 165,699,623-165,703,880 C6orf118
    nsv6637055copy number variation1nstd102humanUncertain significance GRCh37 chr6: 165,541,184-165,841,729 , GRCh38.p12 chr6: 165,127,695-165,428,241 PDE10A, RNA5SP226, 3 more genes
    nsv6636943copy number variation1nstd102humanUncertain significance GRCh37 chr6: 165,246,761-166,028,840 , GRCh38.p12 chr6: 164,833,272-165,615,352 C6orf118, LOC105378116, 3 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
    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
    nsv6631213copy number variation1nstd224human GRCh37 chr6: 165,673,747-165,765,865 , GRCh38.p12 chr6: 165,260,258-165,352,376 PDE10A, C6orf118, 1 more genes
    nsv6617798copy number variation1nstd223human GRCh38 chr6: 165,289,001-165,290,300 , GRCh37.p13 chr6: 165,702,490-165,703,789 C6orf118
    nsv6614874copy number variation1nstd223human GRCh38 chr6: 165,279,748-165,286,103 , GRCh37.p13 chr6: 165,693,237-165,699,592 C6orf118
    nsv6602972copy number variation1nstd223human GRCh38 chr6: 165,309,801-165,318,600 , GRCh37.p13 chr6: 165,723,290-165,732,089 C6orf118, LOC105378113
    nsv6602095copy number variation1nstd223human GRCh38 chr6: 165,286,134-165,290,391 , GRCh37.p13 chr6: 165,699,623-165,703,880 C6orf118
    nsv6556844inversion1nstd223human GRCh38 chr6: 161,649,493-166,382,472 , GRCh37.p13 chr6: 162,070,525-166,795,960 RNU6-730P, TRE-TTC15-1, 49 more genes
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