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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5667399inversion1nstd207human GRCh38 chr2: 108,527,822-109,733,036 , GRCh37.p13 chr2: 109,144,278-110,490,613 , LIMS1, 20 more genes
    nsv5624258insertion1nstd207human GRCh38 chr2: 108,750,602-108,750,602 , GRCh37.p13 chr2: 109,367,058-109,367,058 RANBP2
    nsv5622956insertion1nstd207human GRCh38 chr2: 108,748,004-108,748,004 , GRCh37.p13 chr2: 109,364,460-109,364,460 RANBP2
    nsv5605614insertion1nstd207human GRCh38 chr2: 108,737,799-108,737,799 , GRCh37.p13 chr2: 109,354,255-109,354,255 RANBP2
    nsv5583639copy number variation1nstd207human GRCh38 chr2: 108,726,419-108,727,228 , GRCh37.p13 chr2: 109,342,875-109,343,684 RANBP2
    nsv5581210copy number variation1nstd207human GRCh38 chr2: 108,752,738-108,752,819 , GRCh37.p13 chr2: 109,369,194-109,369,275 RANBP2
    nsv5570596copy number variation1nstd207human GRCh38 chr2: 108,754,173-108,754,236 , GRCh37.p13 chr2: 109,370,629-109,370,692 RANBP2
    nsv5566806copy number variation1nstd207human GRCh38 chr2: 108,726,263-108,726,341 , GRCh37.p13 chr2: 109,342,719-109,342,797 RANBP2
    nsv5566403copy number variation1nstd207human GRCh38 chr2: 108,762,879-108,763,533 , GRCh37.p13 chr2: 109,379,335-109,379,989 RANBP2
    nsv5564425copy number variation1nstd102humanUncertain significance GRCh37 chr2: 108,604,612-109,336,154 , GRCh38.p12 chr2: 107,988,156-108,719,698 LIMS1-AS1, SETD6P1, 18 more genes
    nsv5564250copy number variation1nstd102humanUncertain significance GRCh37 chr2: 109,336,063-109,547,470 , GRCh38.p12 chr2: 108,719,607-108,931,014 EDAR, RANBP2, 2 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5453106copy number variation1nstd206human GRCh38 chr2: 108,741,304-108,741,613 , GRCh37.p13 chr2: 109,357,760-109,358,069 RANBP2
    nsv5449966copy number variation1nstd206human GRCh38 chr2: 108,741,299-108,742,089 , GRCh37.p13 chr2: 109,357,755-109,358,545 RANBP2
    nsv5381336copy number variation1nstd102humanUncertain significance GRCh37 chr2: 109,336,063-109,579,739 , GRCh38.p12 chr2: 108,719,607-108,963,283 RPL39P16, EDAR, 2 more genes
    nsv5381326copy number variation1nstd102humanUncertain significance GRCh37 chr2: 109,356,925-109,357,157 , GRCh38.p12 chr2: 108,740,469-108,740,701 RANBP2
    nsv5297851copy number variation1nstd204human GRCh38.p13 chr2: 108,742,138-109,490,060 , GRCh37.p13 chr2: 109,358,594-110,106,516 , RANBP2, 8 more genes
    nsv5218762copy number variation1nstd204human GRCh38.p13 chr2: 108,769,601-108,770,944 , GRCh37.p13 chr2: 109,386,057-109,387,400 RANBP2
    nsv5206411copy number variation1nstd204human GRCh38.p13 chr2: 108,741,337-108,785,585 , GRCh37.p13 chr2: 109,357,793-109,402,041 CCDC138, RANBP2
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