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Items: 1 to 20 of 883

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
    nsv5883211copy number variation1nstd209human GRCh38 chr1: 145,766,621-145,766,941 , GRCh37.p13 chr1|NW_003871055.3: 2,582,034-2,582,354 , GRCh37.p13 chr1: 145,668,134-145,668,441 RNF115
    nsv5881371copy number variation1nstd209human GRCh38 chr1: 145,648,753-147,971,330 , GRCh37.p13 chr1|NW_003871055.3: 2,464,166-4,786,743 , RNVU1-6, 72 more genes
    nsv5828316copy number variation2nstd209human GRCh38 chr1: 145,776,944-145,778,643 , GRCh37.p13 chr1|NW_003871055.3: 2,592,357-2,594,056 , GRCh37.p13 chr1: 145,656,436-145,658,135 RNF115
    nsv5828315copy number variation2nstd209human GRCh38 chr1: 145,764,662-145,766,793 , GRCh37.p13 chr1: 145,668,273-145,670,400 , GRCh37.p13 chr1|NW_003871055.3: 2,580,075-2,582,206 RNF115
    nsv5828207copy number variation2nstd209human GRCh38 chr1: 145,797,169-145,799,573 , GRCh37.p13 chr1|NW_003871055.3: 2,612,582-2,614,986 , GRCh37.p13 chr1: 145,635,505-145,637,909 RNF115
    nsv5828206copy number variation2nstd209human GRCh38 chr1: 145,790,432-145,809,056 , GRCh37.p13 chr1|NW_003871055.3: 2,605,845-2,624,469 , GRCh37.p13 chr1: 145,626,028-145,644,649 RNF115
    nsv5828205copy number variation2nstd209human GRCh38 chr1: 145,775,544-145,786,547 , GRCh37.p13 chr1: 145,648,532-145,659,531 , GRCh37.p13 chr1|NW_003871055.3: 2,590,957-2,601,960 RNF115
    nsv5828204copy number variation2nstd209human GRCh38 chr1: 145,767,739-145,780,343 , GRCh37.p13 chr1: 145,654,736-145,667,336 , GRCh37.p13 chr1|NW_003871055.3: 2,583,152-2,595,756 RNF115
    nsv5828105copy number variation2nstd209human GRCh38 chr1: 145,812,070-145,821,415 , GRCh37.p13 chr1|NW_003871055.3: 2,627,483-2,636,828 , GRCh37.p13 chr1: 145,613,690-145,623,022 POLR3C, RNF115
    nsv5828104copy number variation2nstd209human GRCh38 chr1: 145,787,698-145,789,581 , GRCh37.p13 chr1: 145,645,500-145,647,383 , GRCh37.p13 chr1|NW_003871055.3: 2,603,111-2,604,994 RNF115
    nsv5828103copy number variation2nstd209human GRCh38 chr1: 145,781,948-145,793,268 , GRCh37.p13 chr1: 145,641,812-145,653,131 , GRCh37.p13 chr1|NW_003871055.3: 2,597,361-2,608,681 RNF115
    nsv5828102copy number variation2nstd209human GRCh38 chr1: 145,768,042-145,769,803 , GRCh37.p13 chr1|NW_003871055.3: 2,583,455-2,585,216 , GRCh37.p13 chr1: 145,665,277-145,667,039 RNF115
    nsv5827997copy number variation2nstd209human GRCh38 chr1: 145,736,153-145,737,352 , GRCh37.p13 chr1|NW_003871055.3: 2,551,566-2,552,765 , GRCh37.p13 chr1: 145,697,735-145,698,934 RNF115, CD160
    nsv5692056mobile element insertion1nstd211human GRCh38 chr1: 145,779,166-145,779,166 , GRCh37.p13 chr1|NW_003871055.3: 2,594,579-2,594,579 , GRCh37.p13 chr1: 145,655,913-145,655,913 RNF115
    nsv5580604copy number variation1nstd207human GRCh38 chr1: 145,809,168-145,809,380 , GRCh37.p13 chr1|NW_003871055.3: 2,624,581-2,624,793 , GRCh37.p13 chr1: 145,625,707-145,625,916 RNF115
    nsv5571855copy number variation1nstd207human GRCh38 chr1: 145,766,942-145,767,068 , GRCh37.p13 chr1|NW_003871055.3: 2,582,355-2,582,481 , GRCh37.p13 chr1: 145,668,007-145,668,133 RNF115
    nsv5565653copy number variation1nstd207human GRCh38 chr1: 145,766,666-145,766,803 , GRCh37.p13 chr1: 145,668,272-145,668,396 , GRCh37.p13 chr1|NW_003871055.3: 2,582,079-2,582,216 RNF115
    nsv5564405copy number variation4nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 145,414,782-145,610,584 , GRCh38.p12 chr1: 145,824,529-146,020,231 MIR6736, POLR3GL, 15 more genes
    nsv5426296copy number variation1nstd206human GRCh37.p13 chr1|NW_003871055.3: 2,318,000-2,634,000 , GRCh38 chr1: 145,502,587-145,818,587 , GRCh37.p13 chr1: 145,616,505-145,833,118 PDZK1, CD160, 4 more genes
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