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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
    nsv7077895inversion1nstd229human GRCh38 chr20: 265,739-1,834,868 , GRCh37.p13 chr20: 246,380-1,815,514 PSMF1, LOC105372498, 46 more genes
    nsv7070620inversion1nstd229human GRCh38 chr20: 805,790-912,627 , GRCh37.p13 chr20: 786,433-893,270 RPS10P5, ANGPT4, 2 more genes
    nsv7017506copy number variation1nstd229human GRCh38 chr20: 803,001-868,700 , GRCh37.p13 chr20: 783,644-849,343 ANGPT4, FAM110A, 1 more genes
    nsv7017282copy number variation1nstd229human GRCh38 chr20: 891,464-951,648 , GRCh37.p13 chr20: 872,107-932,291 ANGPT4, LOC105372492
    nsv7017157copy number variation1nstd229human GRCh38 chr20: 864,569-1,161,607 , GRCh37.p13 chr20: 845,212-1,142,251 ACTG1P3, PSMF1, 4 more genes
    nsv7012460copy number variation1nstd229human GRCh38 chr20: 804,616-936,998 , GRCh37.p13 chr20: 785,259-917,641 ANGPT4, RPS10P5, 2 more genes
    nsv7008595copy number variation1nstd229human GRCh38 chr20: 889,100-893,362 , GRCh37.p13 chr20: 869,743-874,005 ANGPT4
    nsv7007834copy number variation1nstd229human GRCh38 chr20: 208,997-952,202 , GRCh37.p13 chr20: 189,638-932,845 TBC1D20, NRSN2-AS1, 19 more genes
    nsv7007188copy number variation1nstd229human GRCh38 chr20: 915,523-925,865 , GRCh37.p13 chr20: 896,166-906,508 LOC105372492, ANGPT4
    nsv7006541copy number variation1nstd229human GRCh38 chr20: 884,312-909,610 , GRCh37.p13 chr20: 864,955-890,253 ANGPT4
    nsv7006338copy number variation1nstd229human GRCh38 chr20: 843,247-1,354,687 , GRCh37.p13 chr20: 823,890-1,335,331 SDCBP2, FKBP1A-SDCBP2, 12 more genes
    nsv7005662copy number variation1nstd229human GRCh38 chr20: 827,849-903,298 , GRCh37.p13 chr20: 808,492-883,941 FAM110A, ANGPT4, 1 more genes
    nsv7005511copy number variation1nstd229human GRCh38 chr20: 858,901-876,600 , GRCh37.p13 chr20: 839,544-857,243 ANGPT4
    nsv7005318copy number variation1nstd229human GRCh38 chr20: 726,662-885,250 , GRCh37.p13 chr20: 707,306-865,893 RPS10P5, ANGPT4, 2 more genes
    nsv7004500copy number variation1nstd229human GRCh38 chr20: 893,509-905,879 , GRCh37.p13 chr20: 874,152-886,522 ANGPT4
    nsv7004081copy number variation1nstd229human GRCh38 chr20: 671,654-909,508 , GRCh37.p13 chr20: 652,298-890,151 RPS10P5, ANGPT4, 3 more genes
    nsv7003700copy number variation1nstd229human GRCh38 chr20: 891,441-895,484 , GRCh37.p13 chr20: 872,084-876,127 ANGPT4
    nsv7003475copy number variation1nstd229human GRCh38 chr20: 837,675-876,212 , GRCh37.p13 chr20: 818,318-856,855 RPS10P5, ANGPT4, 1 more genes
    nsv7002941copy number variation1nstd229human GRCh38 chr20: 900,820-900,884 , GRCh37.p13 chr20: 881,463-881,527 ANGPT4
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