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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
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 more genes
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7074791inversion1nstd229human GRCh38 chr20: 62,663,291-62,780,773 , GRCh37.p13 chr20: 61,294,643-61,412,125 , NTSR1, 3 more genes
    nsv7069302inversion1nstd229human GRCh38 chr20: 62,502,592-62,836,552 , GRCh37.p13 chr20: 61,267,734-61,467,904 , MIR1-1, 16 more genes
    nsv7064962inversion1nstd229human GRCh38 chr20: 62,710,955-62,963,614 , GRCh37.p13 chr20: 61,342,307-61,594,966 , GID8, 14 more genes
    nsv7063134inversion1nstd229human GRCh38 chr20: 62,739,585-62,856,358 , GRCh37.p13 chr20: 61,370,937-61,487,710 , OGFR-AS1, 8 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
    nsv7036913copy number variation1nstd229human GRCh38 chr20: 62,697,404-62,775,235 , GRCh37.p13 chr20: 61,328,756-61,406,587 , LINC00659, 1 more genes
    nsv7036023copy number variation1nstd229human GRCh38 chr20: 62,765,778-62,778,000 , GRCh37.p13 chr20: 61,397,130-61,409,352 , LINC00659
    nsv7034270copy number variation1nstd229human GRCh38 chr20: 62,773,471-62,775,249 , GRCh37.p13 chr20: 61,404,823-61,406,601 , LINC00659
    nsv7034106copy number variation1nstd229human GRCh38 chr20: 62,767,501-62,875,500 , GRCh37.p13 chr20: 61,398,853-61,506,852 , COL9A3, 9 more genes
    nsv7032680copy number variation1nstd229human GRCh38 chr20: 62,773,172-62,778,225 , GRCh37.p13 chr20: 61,404,524-61,409,577 , LINC00659
    nsv7031791copy number variation1nstd229human GRCh38 chr20: 62,506,495-62,779,553 , GRCh37.p13 chr20: 61,267,734-61,410,905 , MIR1-1HG, 11 more genes
    nsv7031709copy number variation1nstd229human GRCh38 chr20: 62,747,153-62,782,597 , GRCh37.p13 chr20: 61,378,505-61,413,949 , LOC105372716, 2 more genes
    nsv7030939copy number variation1nstd229human GRCh38 chr20: 62,764,801-62,783,500 , GRCh37.p13 chr20: 61,396,153-61,414,852 , LOC105372716, 1 more genes
    nsv7029237copy number variation1nstd229human GRCh38 chr20: 62,545,258-62,783,225 , GRCh37.p13 chr20: 61,267,734-61,414,577 , LOC105372716, 11 more genes
    nsv7028420copy number variation1nstd229human GRCh38 chr20: 62,772,501-62,775,100 , GRCh37.p13 chr20: 61,403,853-61,406,452 , LINC00659
    nsv7024541copy number variation1nstd229human GRCh38 chr20: 62,776,829-62,776,909 , GRCh37.p13 chr20: 61,408,181-61,408,261 , LINC00659
    nsv7024063copy number variation1nstd229human GRCh38 chr20: 62,637,909-62,844,696 , GRCh37.p13 chr20: 61,269,261-61,476,048 , OGFR-AS1, 11 more genes
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