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Items: 1 to 20 of 329

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5900796copy number variation1nstd209human GRCh38 chr3: 155,761,843-155,795,689 , GRCh37.p13 chr3: 155,479,632-155,513,478 C3orf33
    nsv5890356copy number variation1nstd209human GRCh38 chr3: 155,780,984-155,781,266 , GRCh37.p13 chr3: 155,498,773-155,499,055 C3orf33
    nsv5834380copy number variation1nstd209human GRCh38 chr3: 155,761,842-155,782,627 , GRCh37.p13 chr3: 155,479,631-155,500,416 C3orf33
    nsv5693501mobile element insertion1nstd211human GRCh38 chr3: 155,779,859-155,779,859 , GRCh37.p13 chr3: 155,497,648-155,497,648 C3orf33
    nsv5453109copy number variation1nstd206human GRCh38 chr3: 155,761,843-155,795,690 , GRCh37.p13 chr3: 155,479,632-155,513,479 C3orf33
    nsv5450358copy number variation1nstd206human GRCh38 chr3: 155,779,904-155,781,059 , GRCh37.p13 chr3: 155,497,693-155,498,848 C3orf33
    nsv5448775copy number variation1nstd206human GRCh38 chr3: 155,780,994-155,781,267 , GRCh37.p13 chr3: 155,498,783-155,499,056 C3orf33
    nsv5445714copy number variation1nstd206human GRCh38 chr3: 154,528,533-156,057,304 , GRCh37.p13 chr3: 154,246,322-155,775,093 LINC01487, MME, 21 more genes
    nsv5445441copy number variation1nstd206human GRCh38 chr3: 155,780,712-155,780,797 , GRCh37.p13 chr3: 155,498,501-155,498,586 C3orf33
    nsv5439886copy number variation1nstd206human GRCh38 chr3: 155,777,395-155,781,180 , GRCh37.p13 chr3: 155,495,184-155,498,969 C3orf33
    nsv5439373copy number variation1nstd206human GRCh38 chr3: 155,781,466-155,785,880 , GRCh37.p13 chr3: 155,499,255-155,503,669 C3orf33
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5352066translocation1nstd200human GRCh38 chr3: 155,770,172-155,770,172 , GRCh38 chr3: 155,770,351-155,770,351 , GRCh37.p13 chr3: 155,488,140-155,488,140 , GRCh37.p13 chr3: 155,487,961-155,487,961 C3orf33
    nsv5312139copy number variation1nstd204human GRCh38.p13 chr3: 155,761,841-155,795,692 , GRCh37.p13 chr3: 155,479,630-155,513,481 C3orf33
    nsv5239963copy number variation1nstd204human GRCh38.p13 chr3: 155,775,037-155,777,136 , GRCh37.p13 chr3: 155,492,826-155,494,925 C3orf33
    nsv5233899copy number variation1nstd204human GRCh38.p13 chr3: 155,789,278-155,790,277 , GRCh37.p13 chr3: 155,507,067-155,508,066 C3orf33
    nsv5230222copy number variation1nstd204human GRCh38.p13 chr3: 155,777,601-155,782,000 , GRCh37.p13 chr3: 155,495,390-155,499,789 C3orf33
    nsv5229528copy number variation1nstd204human GRCh38.p13 chr3: 155,801,128-155,803,370 , GRCh37.p13 chr3: 155,518,917-155,521,159 C3orf33
    nsv5228504copy number variation1nstd204human GRCh38.p13 chr3: 155,786,650-155,794,652 , GRCh37.p13 chr3: 155,504,439-155,512,441 C3orf33
    nsv5227632copy number variation1nstd204human GRCh38.p13 chr3: 155,760,180-155,795,302 , GRCh37.p13 chr3: 155,477,969-155,513,091 RPL7AP24, C3orf33
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