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Items: 1 to 20 of 153

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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
    nsv7061882inversion1nstd229human GRCh38 chr20: 57,407,587-57,407,691 , GRCh37.p13 chr20: 55,982,643-55,982,747 RBM38
    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
    nsv7033299copy number variation1nstd229human GRCh38 chr20: 57,393,334-57,407,541 , GRCh37.p13 chr20: 55,968,390-55,982,597 RBM38-AS1, RBM38
    nsv7032452copy number variation1nstd229human GRCh38 chr20: 57,397,043-57,407,544 , GRCh37.p13 chr20: 55,972,099-55,982,600 RBM38
    nsv7029546copy number variation1nstd229human GRCh38 chr20: 57,399,984-57,413,559 , GRCh37.p13 chr20: 55,975,040-55,988,615 RBM38
    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
    nsv7019437copy number variation1nstd229human GRCh38 chr20: 57,402,594-57,420,619 , GRCh37.p13 chr20: 55,977,650-55,995,675 RBM38
    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
    nsv6314630complex chromosomal rearrangement3nstd102humanLikely pathogenic GRCh37 chr20: 55,982,643-55,982,643 , GRCh37 chr20: 55,982,746-55,982,746 , GRCh37 chr20: 55,982,746-55,982,746 , GRCh37 chr20: 55,984,328-55,984,328 , GRCh38.p12 chr20: 57,407,587-57,407,587 , GRCh38.p12 chr20: 57,407,690-57,407,690 , GRCh38.p12 chr20: 57,407,690-57,407,690 , GRCh38.p12 chr20: 57,409,272-57,409,272 , GRCh37 chr11: 73,839,840-73,839,840 , GRCh37 chr11: 73,841,465-73,841,465 , GRCh38.p12 chr11: 74,128,795-74,128,795 , GRCh38.p12 chr11: 74,130,420-74,130,420 C2CD3, RBM38
    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
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