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Items: 1 to 20 of 101

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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
    nsv7098911copy number variation1nstd102humanUncertain significance GRCh38 chr20: 21,386,174-21,530,996 , GRCh37.p13 chr20: 21,366,812-21,511,634 GSTM3P1, LOC112268271, 6 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
    nsv6529582copy number variation1nstd223human GRCh38 chr20: 21,389,701-21,395,900 , GRCh37.p13 chr20: 21,370,339-21,376,538 LOC105372558, XRN2, 1 more genes
    nsv6525978copy number variation1nstd223human GRCh38 chr20: 21,033,639-22,376,670 , GRCh37.p13 chr20: 21,014,280-22,357,308 LOC105372561, KIZ, 22 more genes
    nsv6520160copy number variation1nstd223human GRCh38 chr20: 21,395,201-21,397,600 , GRCh37.p13 chr20: 21,375,839-21,378,238 NKX2-4, LOC105372558
    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
    nsv6291762copy number variation1nstd102humanUncertain significance GRCh37 chr20: 21,098,319-21,512,672 , GRCh38.p12 chr20: 21,117,678-21,532,034 RN7SKP140, XRN2, 11 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
    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
    nsv6133907copy number variation1nstd213human GRCh37 chr20: 21,310,000-21,490,001 , GRCh38.p12 chr20: 21,329,362-21,509,363 NKX2-2, XRN2, 6 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
    nsv4457709copy number variation1nstd102humanUncertain significance GRCh37 chr20: 20,817,608-21,771,865 , GRCh38.p12 chr20: 20,836,965-21,791,227 LOC112268271, RPS15AP1, 19 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
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