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Items: 1 to 20 of 211

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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
    nsv7096069copy number variation1nstd102humanUncertain significance GRCh37 chr20: 13,795,054-13,799,077 , GRCh38.p12 chr20: 13,814,408-13,818,431 NDUFAF5
    nsv7096068copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,782,122-13,782,529 , GRCh38.p12 chr20: 13,801,476-13,801,883 NDUFAF5
    nsv7096067copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,775,474-13,775,597 , GRCh38.p12 chr20: 13,794,828-13,794,951 NDUFAF5
    nsv7096014copy number variation1nstd102humanUncertain significance GRCh37 chr20: 13,765,715-15,124,933 , GRCh38.p12 chr20: 13,785,069-15,144,287 NDUFAF5, MACROD2, 15 more genes
    nsv7095875copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,765,715-14,308,152 , GRCh38.p12 chr20: 13,785,069-14,327,506 MACROD2, NDUFAF5, 8 more genes
    nsv7095544copy number variation1nstd102humanPathogenic GRCh37 chr20: 13,765,662-13,775,597 , GRCh38.p12 chr20: 13,785,016-13,794,951 ESF1, NDUFAF5
    nsv7093333copy number variation1nstd102humanPathogenic GRCh38 chr20: 13,785,116-13,785,203 , GRCh37 chr20: 13,765,762-13,765,849 ESF1, NDUFAF5
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7071509inversion1nstd229human GRCh38 chr20: 13,031,496-14,085,882 , GRCh37.p13 chr20: 13,012,144-14,066,528 SEL1L2, GAPDHP2, 12 more genes
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 more genes
    nsv7036923copy number variation1nstd229human GRCh38 chr20: 13,778,401-13,785,900 , GRCh37.p13 chr20: 13,759,047-13,766,546 NDUFAF5, ESF1
    nsv7035512copy number variation1nstd229human GRCh38 chr20: 13,808,318-13,808,694 , GRCh37.p13 chr20: 13,788,964-13,789,340 NDUFAF5
    nsv7035336copy number variation1nstd229human GRCh38 chr20: 13,413,089-13,829,470 , GRCh37.p13 chr20: 13,393,736-13,810,116 ESF1, TASP1, 1 more genes
    nsv7034814copy number variation1nstd229human GRCh38 chr20: 12,459,836-14,234,108 , GRCh37.p13 chr20: 12,440,484-14,214,754 LINC01722, RNU6-278P, 20 more genes
    nsv7031773copy number variation1nstd229human GRCh38 chr20: 13,451,886-13,854,849 , GRCh37.p13 chr20: 13,432,533-13,835,495 TASP1, SEL1L2, 2 more genes
    nsv7029091copy number variation1nstd229human GRCh38 chr20: 13,757,301-13,789,800 , GRCh37.p13 chr20: 13,737,948-13,770,446 NDUFAF5, ESF1
    nsv7026011copy number variation1nstd229human GRCh38 chr20: 13,777,383-13,784,168 , GRCh37.p13 chr20: 13,758,029-13,764,814 NDUFAF5, ESF1
    nsv7025742copy number variation1nstd229human GRCh38 chr20: 13,592,501-14,233,642 , GRCh37.p13 chr20: 13,573,148-14,214,288 RPS3P1, RNU6-278P, 8 more genes
    nsv7022879copy number variation1nstd229human GRCh38 chr20: 13,793,901-13,808,400 , GRCh37.p13 chr20: 13,774,547-13,789,046 NDUFAF5
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