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Items: 1 to 20 of 112

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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
    nsv7095879copy number variation2nstd102humanUncertain significance GRCh37 chr20: 1,959,939-6,760,201 , GRCh38.p12 chr20: 1,979,293-6,779,554 SLC23A2, TARDBPP1, 120 more genes
    nsv7074371inversion1nstd229human GRCh38 chr20: 2,515,505-5,510,656 , GRCh37.p13 chr20: 2,496,151-5,491,302 RPL19P1, DDRGK1, 87 more genes
    nsv7068018inversion1nstd229human GRCh38 chr20: 1,903,309-3,817,737 , GRCh37.p13 chr20: 1,883,955-3,798,384 PCED1A, UBOX5-AS1, 62 more genes
    nsv7006475copy number variation1nstd229human GRCh38 chr20: 2,789,947-2,796,715 , GRCh37.p13 chr20: 2,770,593-2,777,361 CPXM1
    nsv7005540copy number variation1nstd229human GRCh38 chr20: 2,787,995-2,795,248 , GRCh37.p13 chr20: 2,768,641-2,775,894 CPXM1
    nsv7004698copy number variation1nstd229human GRCh38 chr20: 2,778,405-2,808,129 , GRCh37.p13 chr20: 2,759,051-2,788,775 RPL19P1, CPXM1
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6525554copy number variation1nstd223human GRCh38 chr20: 2,778,405-2,808,128 , GRCh37.p13 chr20: 2,759,051-2,788,774 CPXM1, RPL19P1
    nsv6133803copy number variation1nstd213human GRCh37 chr20: 2,720,000-3,420,001 , GRCh38.p12 chr20: 2,739,354-3,439,354 AVP, GNRH2, 26 more genes
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5329250copy number variation1nstd204human GRCh38.p13 chr20: 2,800,117-2,800,231 , GRCh37.p13 chr20: 2,780,763-2,780,877 CPXM1
    nsv5012175copy number variation1nstd200human GRCh38 chr20: 2,789,947-2,796,710 , GRCh37.p13 chr20: 2,770,593-2,777,356 CPXM1
    nsv4861661copy number variation1nstd200human GRCh37 chr20: 2,770,593-2,777,356 , GRCh38.p12 chr20: 2,789,947-2,796,710 CPXM1
    nsv4457667copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,738,670-3,054,217 , GRCh38.p12 chr20: 2,758,024-3,073,571 CPXM1, RPL19P1, 10 more genes
    nsv4422729copy number variation1nstd174human GRCh37 chr20: 2,631,269-2,970,332 , GRCh38.p12 chr20: 2,650,623-2,989,686 , VPS16, 17 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
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 more genes
    nsv3968363copy number variation1nstd168human GRCh38 chr20: 2,793,342-2,844,769 , GRCh37.p13 chr20: 2,773,988-2,825,415 VPS16, CPXM1, 3 more genes
    nsv3923490copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-13,029,401 , NCBI36 chr20: 8,747-12,958,049 , GRCh37 chr20: 60,747-13,010,049 LINC01751, RNA5SP474, 238 more genes
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