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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6279080copy number variation1nstd214human GRCh38 chr20: 29,474,641-29,474,707 , GRCh37.p13 chr: NaN-NaN FRG1EP
    nsv5973864inversion1nstd209human GRCh38 chr20: 29,104,721-29,868,830 , GRCh37.p13 chr9: 66,459,367-68,422,752 FRG2EP, AGGF1P10, 18 more genes
    nsv5966877copy number variation1nstd209human GRCh38 chr20: 29,125,619-30,424,446 , GRCh37.p13 chr20: 25,864,401-29,615,130 DUX4L33, LOC105379476, 27 more genes
    nsv5965062copy number variation1nstd209human GRCh38 chr20: 29,285,033-30,468,916 , GRCh37.p13 chr4: 190,198,664-190,843,361 , GRCh37.p13 chr20: 25,864,401-29,615,130 LOC110467538, RNA5SP532, 27 more genes
    nsv5958416copy number variation1nstd209human GRCh38 chr20: 29,350,778-29,788,349 , GRCh37.p13 chr: NaN-NaN RARRES2P11, FRG1EP, 12 more genes
    nsv5958242copy number variation1nstd209human GRCh38 chr20: 29,300,713-29,742,883 , GRCh37.p13 chr: NaN-NaN DUX4L33, DUX4L34, 14 more genes
    nsv5956670copy number variation1nstd209human GRCh38 chr20: 29,327,704-29,764,880 , GRCh37.p13 chr: NaN-NaN FAM242B, DUX4L36, 12 more genes
    nsv5955838copy number variation1nstd209human GRCh38 chr20: 25,923,975-30,219,168 , GRCh37.p13 chr20: 25,904,611-29,453,844 CDC27P3, LOC105379477, 30 more genes
    nsv5954916copy number variation1nstd209human GRCh38 chr20: 29,108,114-30,407,063 , GRCh37.p13 chr20: 25,864,401-29,615,130 , GRCh37.p13 chr9: 66,459,367-68,422,752 LOC110467522, LOC105379476, 27 more genes
    nsv5952980copy number variation1nstd209human GRCh38 chr20: 28,864,857-29,847,494 , GRCh37.p13 chr20: 25,864,401-29,615,130 , GRCh37.p13 chr9: 66,459,367-68,486,942 FRG2EP, LOC110467522, 19 more genes
    nsv5948031copy number variation1nstd209human GRCh38 chr20: 29,361,988-29,799,580 , GRCh37.p13 chr: NaN-NaN LOC105379477, RARRES2P11, 12 more genes
    nsv5887062copy number variation2nstd209human GRCh38 chr20: 29,490,200-29,496,222 , GRCh37.p13 chr22|NT_167235.1: 24,832-27,855 FRG1EP
    nsv5886426copy number variation1nstd209human GRCh38 chr20: 29,475,186-29,477,586 , GRCh37.p13 chrUn|NT_167213.1: 72,662-75,070 FRG1EP
    nsv5884058copy number variation1nstd209human GRCh38 chr20: 29,472,884-29,477,586 , GRCh37.p13 chrUn|NT_167213.1: 70,364-75,070 FRG1EP
    nsv5881825copy number variation1nstd209human GRCh38 chr20: 29,480,105-29,481,220 , GRCh37.p13 chrUn|NT_167213.1: 77,592-78,705 FRG1EP
    nsv5881569copy number variation1nstd209human GRCh38 chr20: 29,480,103-29,485,117 , GRCh37.p13 chrUn|NT_167213.1: 77,590-81,799 FRG1EP
    nsv5880698copy number variation2nstd209human GRCh38 chr20: 29,485,424-29,493,040 , GRCh37.p13 chr22|NT_167235.1: 20,082-27,618 FRG1EP
    nsv5872431copy number variation1nstd209human GRCh38 chr20: 29,476,430-29,477,586 , GRCh37.p13 chrUn|NT_167213.1: 73,908-75,070 FRG1EP
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