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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
    nsv7096267copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,471,874-61,472,084 , GRCh38.p12 chr20: 62,840,522-62,840,732 TCFL5, COL9A3
    nsv7096266copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,448,417-61,472,084 , GRCh38.p12 chr20: 62,817,065-62,840,732 COL9A3, TCFL5
    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
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 LINC01749, HAR1A, 32 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
    nsv7036153copy number variation1nstd229human GRCh38 chr20: 62,859,401-62,861,200 , GRCh37.p13 chr20: 61,490,753-61,492,552 LOC105372717, TCFL5
    nsv7034106copy number variation1nstd229human GRCh38 chr20: 62,767,501-62,875,500 , GRCh37.p13 chr20: 61,398,853-61,506,852 , COL9A3, 9 more genes
    nsv7025373copy number variation1nstd229human GRCh38 chr20: 62,853,074-62,853,167 , GRCh37.p13 chr20: 61,484,426-61,484,519 TCFL5
    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
    nsv7020490copy number variation1nstd229human GRCh38 chr20: 62,767,801-62,877,700 , GRCh37.p13 chr20: 61,399,153-61,509,052 , DIDO1, 10 more genes
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6598703inversion1nstd223human GRCh38 chr20: 62,855,222-62,855,745 , GRCh37.p13 chr20: 61,486,574-61,487,097 TCFL5
    nsv6550991copy number variation1nstd223human GRCh38 chr20: 62,848,802-62,849,584 , GRCh37.p13 chr20: 61,480,154-61,480,936 TCFL5
    nsv6541478copy number variation1nstd223human GRCh38 chr20: 62,838,963-62,848,776 , GRCh37.p13 chr20: 61,470,315-61,480,128 TCFL5, COL9A3, 1 more genes
    nsv6537398copy number variation1nstd223human GRCh38 chr20: 62,837,835-62,839,411 , GRCh37.p13 chr20: 61,469,187-61,470,763 TCFL5, COL9A3
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
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