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Items: 1 to 20 of 313

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5964838insertion1nstd209human GRCh38 chr2: 26,851,335-26,851,335 , GRCh37.p13 chr2: 27,074,203-27,074,203 DPYSL5
    nsv5948937insertion1nstd209human GRCh38 chr2: 26,928,705-26,928,705 , GRCh37.p13 chr2: 27,151,573-27,151,573 DPYSL5
    nsv5876933copy number variation1nstd209human GRCh38 chr2: 26,887,694-26,887,754 , GRCh37.p13 chr2: 27,110,562-27,110,622 DPYSL5
    nsv5725032mobile element insertion1nstd211human GRCh38 chr2: 26,936,961-26,936,961 , GRCh37.p13 chr2: 27,159,829-27,159,829 DPYSL5
    nsv5715283mobile element insertion2nstd211human GRCh38 chr2: 26,921,456-26,921,456 , GRCh37.p13 chr2: 27,144,324-27,144,324 DPYSL5
    nsv5621793insertion1nstd207human GRCh38 chr2: 26,851,335-26,851,335 , GRCh37.p13 chr2: 27,074,203-27,074,203 DPYSL5
    nsv5620500insertion1nstd207human GRCh38 chr2: 26,856,886-26,856,886 , GRCh37.p13 chr2: 27,079,754-27,079,754 DPYSL5
    nsv5574775copy number variation1nstd207human GRCh38 chr2: 26,932,072-26,932,122 , GRCh37.p13 chr2: 27,154,940-27,154,990 DPYSL5
    nsv5572903copy number variation1nstd207human GRCh38 chr2: 26,887,694-26,887,754 , GRCh37.p13 chr2: 27,110,562-27,110,622 DPYSL5
    nsv5563528mobile element insertion1nstd206human GRCh38 chr2: 26,936,671-26,936,704 , GRCh37.p13 chr2: 27,159,539-27,159,572 DPYSL5
    nsv5557121mobile element insertion1nstd206human GRCh38 chr2: 26,921,456-26,921,507 , GRCh37.p13 chr2: 27,144,324-27,144,375 DPYSL5
    nsv5551368insertion1nstd206human GRCh38 chr2: 26,851,335-26,851,335 , GRCh37.p13 chr2: 27,074,203-27,074,203 DPYSL5
    nsv5449399copy number variation1nstd206human GRCh38 chr2: 26,942,810-26,943,462 , GRCh37.p13 chr2: 27,165,678-27,166,330 DPYSL5
    nsv5443841copy number variation1nstd206human GRCh38 chr2: 26,944,318-26,945,205 , GRCh37.p13 chr2: 27,167,186-27,168,073 DPYSL5
    nsv5439619copy number variation1nstd206human GRCh38 chr2: 26,903,000-26,909,000 , GRCh37.p13 chr2: 27,125,868-27,131,868 DPYSL5
    nsv5436428copy number variation1nstd206human GRCh38 chr2: 26,903,117-26,903,191 , GRCh37.p13 chr2: 27,125,985-27,126,059 DPYSL5
    nsv5289721copy number variation1nstd204human GRCh38.p13 chr2: 26,937,845-26,939,397 , GRCh37.p13 chr2: 27,160,713-27,162,265 DPYSL5
    nsv5214382copy number variation1nstd204human GRCh38.p13 chr2: 26,938,475-26,939,574 , GRCh37.p13 chr2: 27,161,343-27,162,442 DPYSL5
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