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Items: 1 to 20 of 192

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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
    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
    nsv7034106copy number variation1nstd229human GRCh38 chr20: 62,767,501-62,875,500 , GRCh37.p13 chr20: 61,398,853-61,506,852 , COL9A3, 9 more genes
    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
    nsv7020272copy number variation1nstd229human GRCh38 chr20: 62,687,001-62,832,700 , GRCh37.p13 chr20: 61,318,353-61,464,052 , LINC00659, 7 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
    nsv6596690inversion1nstd223human GRCh38 chr20: 62,809,164-62,814,201 , GRCh37.p13 chr20: 61,440,516-61,445,553 OGFR
    nsv6540715copy number variation1nstd223human GRCh38 chr20: 62,795,468-62,804,189 , GRCh37.p13 chr20: 61,426,820-61,435,541 OGFR-AS1, OGFR, 1 more genes
    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
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6290337copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,038,552-62,907,579 , GRCh38.p12 chr20: 62,463,496-64,276,226 CHRNA4, COL9A3, 99 more genes
    nsv6290297copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,041,481-62,680,992 , GRCh38.p12 chr20: 62,466,425-64,049,639 CHRNA4, COL9A3, 91 more genes
    nsv6290296copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 61,273,854-62,907,579 , GRCh38.p12 chr20: 62,642,502-64,276,226 CHRNA4, COL9A3, 90 more genes
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