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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095898copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,223,339-44,638,757 , GRCh38.p12 chr20: 43,594,699-46,010,118 ADA, CCN5, 99 more genes
    nsv7075825inversion1nstd229human GRCh38 chr20: 45,232,922-45,712,689 , GRCh37.p13 chr20: 43,861,563-44,341,328 PIGT, LOC105372630, 33 more genes
    nsv7059679inversion1nstd229human GRCh38 chr20: 45,693,721-45,708,532 , GRCh37.p13 chr20: 44,322,360-44,337,171 WFDC3, MIR3617, 2 more genes
    nsv7058954inversion1nstd229human GRCh38 chr20: 45,701,075-45,708,237 , GRCh37.p13 chr20: 44,329,714-44,336,876 MIR3617, WFDC10B, 2 more genes
    nsv7023667copy number variation1nstd229human GRCh38 chr20: 45,681,214-45,684,077 , GRCh37.p13 chr20: 44,309,853-44,312,716 WFDC10B
    nsv6626779copy number variation1nstd224human GRCh37 chr20: 44,334,536-44,380,269 , GRCh38.p12 chr20: 45,705,897-45,751,630 WFDC3, SPINT5P, 4 more genes
    nsv6626778copy number variation1nstd224human GRCh37 chr20: 44,334,536-44,378,173 , GRCh38.p12 chr20: 45,705,897-45,749,534 WFDC3, SPINT5P, 4 more genes
    nsv6626705copy number variation3nstd224human GRCh37 chr20: 44,336,716-44,380,269 , GRCh38.p12 chr20: 45,708,077-45,751,630 WFDC3, SPINT5P, 4 more genes
    nsv6626704copy number variation2nstd224human GRCh37 chr20: 44,336,716-44,378,173 , GRCh38.p12 chr20: 45,708,077-45,749,534 WFDC3, SPINT5P, 4 more genes
    nsv6626703copy number variation1nstd224human GRCh37 chr20: 44,333,559-44,378,173 , GRCh38.p12 chr20: 45,704,920-45,749,534 WFDC3, SPINT5P, 5 more genes
    nsv6595743inversion1nstd223human GRCh38 chr20: 45,693,721-45,708,532 , GRCh37.p13 chr20: 44,322,360-44,337,171 WFDC3, WFDC13, 2 more genes
    nsv6553294copy number variation1nstd223human GRCh38 chr20: 45,703,173-45,703,937 , GRCh37.p13 chr20: 44,331,812-44,332,576 WFDC13, MIR3617, 1 more genes
    nsv6553076copy number variation1nstd223human GRCh38 chr20: 45,701,912-45,702,535 , GRCh37.p13 chr20: 44,330,551-44,331,174 WFDC10B, WFDC13
    nsv6545726copy number variation1nstd223human GRCh38 chr20: 45,693,720-45,701,074 , GRCh37.p13 chr20: 44,322,359-44,329,713 WFDC10B, WFDC13
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6134165copy number variation1nstd213human GRCh37 chr20: 44,320,000-45,430,001 , GRCh38.p12 chr20: 45,691,361-46,801,362 MMP9, MKRN7P, 39 more genes
    nsv6134034copy number variation1nstd213human GRCh37 chr20: 44,070,000-44,320,001 , GRCh38.p12 chr20: 45,441,360-45,691,362 EPPIN, RPL5P2, 15 more genes
    nsv6133816copy number variation1nstd213human GRCh37 chr20: 43,650,000-45,170,001 , GRCh38.p12 chr20: 45,021,359-46,541,362 MMP9, PI3, 76 more genes
    nsv5973965insertion1nstd209human GRCh37.p13 chr20: 44,333,710-44,333,710 , GRCh38 chr20: 45,705,071-45,705,071 WFDC13, WFDC10B, 1 more genes
    nsv5667059inversion1nstd207human GRCh37.p13 chr20: 44,336,707-44,371,085 , GRCh38 chr20: 45,708,068-45,742,446 WFDC3, WFDC13, 2 more genes
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