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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 more genes
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7015435copy number variation1nstd229human GRCh38 chr20: 4,445,183-5,667,683 , GRCh37.p13 chr20: 4,425,830-5,648,329 LOC107985411, LOC105372510, 26 more genes
    nsv7008977copy number variation1nstd229human GRCh38 chr20: 4,351,306-5,587,282 , GRCh37.p13 chr20: 4,331,953-5,567,928 LINC00658, GPCPD1, 26 more genes
    nsv7006305copy number variation1nstd229human GRCh38 chr20: 3,792,209-4,972,873 , GRCh37.p13 chr20: 3,772,856-4,953,519 MIR103A2, LOC107985392, 23 more genes
    nsv6626572copy number variation1nstd224human GRCh37 chr20: 4,155,880-5,165,596 , GRCh38.p12 chr20: 4,175,233-5,184,950 SMOX, PRNT, 18 more genes
    nsv6531113copy number variation1nstd223human GRCh38 chr20: 4,667,186-4,730,574 , GRCh37.p13 chr20: 4,647,832-4,711,220 PRNP, PRND, 1 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6134036copy number variation1nstd213human GRCh37 chr20: 4,470,000-4,700,001 , GRCh38.p12 chr20: 4,489,352-4,719,355 PRNP, RPS4XP2, 2 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv5934392copy number variation1nstd209human GRCh38 chr20: 3,792,203-4,972,872 , GRCh37.p13 chr20: 3,772,850-4,953,518 FTLP3, PANK2-AS1, 23 more genes
    nsv5033561inversion1nstd200human GRCh38 chr20: 3,693,712-5,966,244 , GRCh37.p13 chr20: 3,674,359-5,946,890 , LOC107985411, 53 more genes
    nsv4729947copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,092,739-4,939,933 , GRCh38.p12 chr20: 3,112,093-4,959,287 SF3A3P1, PRND, 46 more genes
    nsv4676210copy number variation1nstd102humanUncertain significance GRCh37 chr20: 4,439,086-4,676,435 , GRCh38.p12 chr20: 4,458,439-4,695,789 RPS4XP2, PRNP, 2 more genes
    nsv4627216copy number variation1nstd183human GRCh37 chr20: 4,333,427-4,776,533 , GRCh38.p12 chr20: 4,352,780-4,795,887 PRNP, RASSF2, 7 more genes
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