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Items: 1 to 20 of 113

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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
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7036487copy number variation1nstd229human GRCh38 chr20: 10,449,828-13,745,757 , GRCh37.p13 chr20: 10,430,476-13,726,404 RN7SKP111, MIR6870, 36 more genes
    nsv7023247copy number variation1nstd229human GRCh38 chr20: 11,023,928-11,027,359 , GRCh37.p13 chr20: 11,004,576-11,008,007 LINC02871
    nsv7022067copy number variation1nstd229human GRCh38 chr20: 7,868,752-11,491,709 , GRCh37.p13 chr20: 7,849,399-11,472,357 LOC339593, LOC105372522, 36 more genes
    nsv7019992copy number variation1nstd229human GRCh38 chr20: 11,022,732-11,035,400 , GRCh37.p13 chr20: 11,003,380-11,016,048 LINC02871
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6528492copy number variation1nstd223human GRCh38 chr20: 11,027,501-11,072,700 , GRCh37.p13 chr20: 11,008,149-11,053,348 LINC02871
    nsv6519981copy number variation1nstd223human GRCh38 chr20: 11,023,923-11,027,358 , GRCh37.p13 chr20: 11,004,571-11,008,006 LINC02871
    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
    nsv6251238mobile element insertion1nstd215human GRCh38 chr20: 11,024,855-11,024,855 , GRCh37.p13 chr20: 11,005,503-11,005,503 LINC02871
    nsv6134010copy number variation1nstd213human GRCh37 chr20: 10,960,000-11,250,001 , GRCh38.p12 chr20: 10,979,352-11,269,353 LOC339593, LINC02871, 2 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv6133792copy number variation1nstd213human GRCh37 chr20: 10,380,000-13,180,001 , GRCh38.p12 chr20: 10,399,352-13,199,354 JAG1, MKKS, 32 more genes
    nsv5697635mobile element insertion1nstd211human GRCh38 chr20: 11,024,855-11,024,855 , GRCh37.p13 chr20: 11,005,503-11,005,503 LINC02871
    nsv5421056mobile element insertion1nstd206human GRCh38 chr20: 11,024,855-11,024,906 , GRCh37.p13 chr20: 11,005,503-11,005,554 LINC02871
    nsv5381139copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,579,323-11,009,878 , GRCh38.p12 chr20: 10,598,675-11,029,230 LOC107985398, MIR6870, 7 more genes
    nsv5360056translocation1nstd200human GRCh38 chr20: 11,028,029-11,028,029 , GRCh38 chr20: 11,027,944-11,027,944 , GRCh37.p13 chr20: 11,008,677-11,008,677 , GRCh37.p13 chr20: 11,008,592-11,008,592 LINC02871
    nsv5012545copy number variation1nstd200human GRCh38 chr20: 11,023,923-11,027,358 , GRCh37.p13 chr20: 11,004,571-11,008,006 LINC02871
    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
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