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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7071269inversion1nstd229human GRCh38 chr20: 51,579,374-58,024,568 , GRCh37.p13 chr20: 50,195,913-56,599,624 CBLN4, LOC105372693, 89 more genes
    nsv7063616inversion1nstd229human GRCh38 chr20: 51,911,434-57,961,609 , GRCh37.p13 chr20: 50,527,973-56,536,665 FAM210B, BCAS1, 81 more genes
    nsv7058989inversion1nstd229human GRCh38 chr20: 52,927,440-57,459,107 , GRCh37.p13 chr20: 51,543,979-56,034,163 FAM210B, RPS4XP3, 61 more genes
    nsv7058267inversion1nstd229human GRCh38 chr20: 51,559,821-57,992,303 , GRCh37.p13 chr20: 50,176,360-56,567,359 LOC105372683, MRPS33P4, 89 more genes
    nsv7037339copy number variation1nstd229human GRCh38 chr20: 57,325,590-57,659,163 , GRCh37.p13 chr20: 55,900,646-56,234,219 CTCFL, HMGB1P1, 13 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7036491copy number variation1nstd229human GRCh38 chr20: 57,238,777-57,406,580 , GRCh37.p13 chr20: 55,813,833-55,981,636 RBM38-AS1, NMTRL-TAA5-1, 10 more genes
    nsv7036177copy number variation1nstd229human GRCh38 chr20: 54,492,617-57,541,251 , GRCh37.p13 chr20: 53,109,156-56,116,307 SPO11, BMP7, 47 more genes
    nsv7035206copy number variation1nstd229human GRCh38 chr20: 57,381,468-57,384,861 , GRCh37.p13 chr20: 55,956,524-55,959,917 RBM38-AS1
    nsv7033299copy number variation1nstd229human GRCh38 chr20: 57,393,334-57,407,541 , GRCh37.p13 chr20: 55,968,390-55,982,597 RBM38-AS1, RBM38
    nsv7031963copy number variation1nstd229human GRCh38 chr20: 57,378,106-57,384,277 , GRCh37.p13 chr20: 55,953,162-55,959,333 RBM38-AS1, RAE1
    nsv7025243copy number variation1nstd229human GRCh38 chr20: 57,381,417-57,384,861 , GRCh37.p13 chr20: 55,956,473-55,959,917 RBM38-AS1
    nsv7024807copy number variation1nstd229human GRCh38 chr20: 56,642,648-58,322,378 , GRCh37.p13 chr20: 55,217,704-56,897,434 MIR4325, LOC105372693, 36 more genes
    nsv7022086copy number variation1nstd229human GRCh38 chr20: 57,392,778-57,407,541 , GRCh37.p13 chr20: 55,967,834-55,982,597 RBM38-AS1, RBM38
    nsv6544397copy number variation1nstd223human GRCh38 chr20: 57,381,467-57,384,860 , GRCh37.p13 chr20: 55,956,523-55,959,916 RBM38-AS1
    nsv6541267copy number variation1nstd223human GRCh38 chr20: 57,374,707-57,401,065 , GRCh37.p13 chr20: 55,949,763-55,976,121 RBM38-AS1, RBM38, 1 more genes
    nsv6314094copy number variation1nstd102humanPathogenic GRCh37 chr20: 55,292,205-57,866,365 , GRCh38.p12 chr20: 56,717,149-59,291,310 PCK1, MIR296, 58 more genes
    nsv6311086copy number variation1nstd102humanUncertain significance GRCh37 chr20: 54,823,900-57,899,514 , GRCh38.p12 chr20: 56,248,844-59,324,459 CTSZ, SPO11, 75 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
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