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Items: 1 to 20 of 102

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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
    nsv7072011inversion1nstd229human GRCh38 chr20: 19,125,473-21,611,699 , GRCh37.p13 chr20: 19,106,117-21,592,337 SLC24A3, GSTM3P1, 35 more genes
    nsv7071751inversion1nstd229human GRCh38 chr20: 20,367,155-21,545,773 , GRCh37.p13 chr20: 20,347,799-21,526,411 ZNF877P, RNA5SP477, 20 more genes
    nsv7029789copy number variation1nstd229human GRCh38 chr20: 20,363,401-20,368,700 , GRCh37.p13 chr20: 20,344,045-20,349,344 INSM1
    nsv6526445copy number variation1nstd223human GRCh38 chr20: 20,363,401-20,370,100 , GRCh37.p13 chr20: 20,344,045-20,350,744 INSM1
    nsv6314164copy number variation1nstd102humanPathogenic GRCh37 chr20: 19,292,925-22,187,397 , GRCh38.p12 chr20: 19,312,281-22,206,759 SLC25A6P1, RPL41P1, 37 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134277copy number variation1nstd213human GRCh37 chr20: 20,290,000-20,510,001 , GRCh38.p12 chr20: 20,309,356-20,529,357 INSM1, CFAP61, 2 more genes
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6134268copy number variation1nstd213human GRCh37 chr20: 13,380,000-22,450,001 , GRCh38.p12 chr20: 13,399,353-22,469,363 BFSP1, INSM1, 134 more genes
    nsv6133797copy number variation1nstd213human GRCh37 chr20: 20,250,000-21,220,001 , GRCh38.p12 chr20: 20,269,356-21,239,363 KIZ, KIZ-AS1, 13 more genes
    nsv5699870mobile element insertion1nstd211human GRCh38 chr20: 20,366,222-20,366,222 , GRCh37.p13 chr20: 20,346,866-20,346,866 INSM1
    nsv5432498mobile element insertion1nstd206human GRCh38 chr20: 20,366,222-20,366,273 , GRCh37.p13 chr20: 20,346,866-20,346,917 INSM1
    nsv5291238copy number variation1nstd204human GRCh38.p13 chr20: 20,327,801-20,409,100 , GRCh37.p13 chr20: 20,308,445-20,389,744 CFAP61, RALGAPA2, 1 more genes
    nsv5025194copy number variation1nstd200human GRCh38 chr20: 20,245,291-20,392,026 , GRCh37.p13 chr20: 20,225,935-20,372,670 , CFAP61, 5 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4676419copy number variation1nstd102humanPathogenic GRCh37 chr20: 8,571,696-22,088,650 , GRCh38.p12 chr20: 8,591,049-22,108,012 PGAM3P, EEF1A1P34, 182 more genes
    nsv4672595copy number variation1nstd186human GRCh37 chr20: 20,343,201-20,351,500 , GRCh38.p12 chr20: 20,362,557-20,370,856 INSM1
    nsv4632168copy number variation1nstd183human GRCh37 chr20: 20,343,201-20,351,500 , GRCh38.p12 chr20: 20,362,557-20,370,856 INSM1
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
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