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Items: 1 to 20 of 133

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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
    nsv7098816copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 3,005,123-5,547,871 , GRCh38.p12 chr20: 3,024,477-5,567,225 ADRA1D, AVP, 70 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
    nsv7095551copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,063,276-3,903,941 , GRCh38.p12 chr20: 3,082,630-3,923,294 PANK2, MAVS, 31 more genes
    nsv7074742inversion1nstd229human GRCh38 chr20: 3,441,683-5,027,331 , GRCh37.p13 chr20: 3,422,330-5,007,977 MAVS, MIR103B2, 33 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
    nsv7063954inversion1nstd229human GRCh38 chr20: 3,693,712-5,966,241 , GRCh37.p13 chr20: 3,674,359-5,946,887 GPCPD1, PANK2, 52 more genes
    nsv7060166inversion1nstd229human GRCh38 chr20: 2,999,965-6,521,256 , GRCh37.p13 chr20: 2,980,611-6,501,903 FASTKD5, LOC101929098, 86 more genes
    nsv7015272copy number variation1nstd229human GRCh38 chr20: 3,519,388-3,799,972 , GRCh37.p13 chr20: 3,500,035-3,780,619 CDC25B, HSPA12B, 7 more genes
    nsv7011061copy number variation1nstd229human GRCh38 chr20: 3,745,501-3,786,200 , GRCh37.p13 chr20: 3,726,148-3,766,847 SPEF1, HSPA12B, 3 more genes
    nsv7007813copy number variation1nstd229human GRCh38 chr20: 3,543,154-3,905,714 , GRCh37.p13 chr20: 3,523,801-3,886,361 LINC01730, HSPA12B, 12 more genes
    nsv7000908copy number variation1nstd229human GRCh38 chr20: 3,643,601-3,786,300 , GRCh37.p13 chr20: 3,624,248-3,766,947 CDC25B, ADAM33, 7 more genes
    nsv6626772copy number variation1nstd224human GRCh37 chr20: 3,765,986-3,776,175 , GRCh38.p12 chr20: 3,785,339-3,795,528 CENPB, CDC25B
    nsv6595692inversion1nstd223human GRCh38 chr20: 2,488,062-4,373,728 , GRCh37.p13 chr20: 2,468,708-4,354,375 PANK2, LOC105372504, 62 more genes
    nsv6533157copy number variation1nstd223human GRCh38 chr20: 3,543,154-3,905,714 , GRCh37.p13 chr20: 3,523,801-3,886,361 ADAM33, PANK2, 12 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6315500copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155 DNAAF9, LOC105372508, 40 more genes
    nsv6283643copy number variation1nstd214human GRCh38 chr20: 3,786,487-3,786,578 , GRCh37.p13 chr20: 3,767,134-3,767,225 CDC25B, CENPB
    nsv6220564copy number variation1nstd214human GRCh38 chr20: 3,786,474-3,786,536 , GRCh37.p13 chr20: 3,767,121-3,767,183 CDC25B, CENPB
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