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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148186copy number variation1nstd102humanUncertain significance GRCh37 chr20: 52,773,668-62,965,020 , GRCh38.p12 chr20: 54,157,129-64,333,667 LOC105372717, CTCFL, 245 more genes
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7035987copy number variation1nstd229human GRCh38 chr20: 62,185,367-62,190,766 , GRCh37.p13 chr20: 60,760,423-60,765,822 MTG2
    nsv7033331copy number variation1nstd229human GRCh38 chr20: 62,179,670-62,187,243 , GRCh37.p13 chr20: 60,754,726-60,762,299 SS18L1, MTG2
    nsv7027089copy number variation1nstd229human GRCh38 chr20: 62,079,701-62,294,500 , GRCh37.p13 chr20: 60,654,757-60,869,556 HRH3, PSMA7, 6 more genes
    nsv7022291copy number variation1nstd229human GRCh38 chr20: 62,181,442-62,181,532 , GRCh37.p13 chr20: 60,756,498-60,756,588 MTG2, SS18L1
    nsv7020543copy number variation1nstd229human GRCh38 chr20: 62,182,285-62,183,746 , GRCh37.p13 chr20: 60,757,341-60,758,802 MTG2, SS18L1
    nsv7020075copy number variation1nstd229human GRCh38 chr20: 62,198,035-62,200,231 , GRCh37.p13 chr20: 60,773,091-60,775,287 MTG2
    nsv6637836copy number variation1nstd102humanUncertain significance GRCh37 chr20: 60,621,074-62,915,555 , GRCh38.p12 chr20: 62,046,018-64,284,202 SLC17A9, MIR3195, 120 more genes
    nsv6597987inversion1nstd223human GRCh38 chr20: 62,183,874-62,186,576 , GRCh37.p13 chr20: 60,758,930-60,761,632 MTG2
    nsv6551754copy number variation1nstd223human GRCh38 chr20: 62,184,154-62,185,209 , GRCh37.p13 chr20: 60,759,210-60,760,265 MTG2
    nsv6549305copy number variation1nstd223human GRCh38 chr20: 62,184,134-62,184,885 , GRCh37.p13 chr20: 60,759,190-60,759,941 MTG2
    nsv6547251copy number variation1nstd223human GRCh38 chr20: 62,195,036-62,202,498 , GRCh37.p13 chr20: 60,770,092-60,777,554 MTG2
    nsv6545303copy number variation1nstd223human GRCh38 chr20: 62,185,367-62,190,768 , GRCh37.p13 chr20: 60,760,423-60,765,824 MTG2
    nsv6541228copy number variation1nstd223human GRCh38 chr20: 62,167,075-62,199,737 , GRCh37.p13 chr20: 60,742,131-60,774,793 MTG2, SS18L1
    nsv6315308copy number variation1nstd102humanUncertain significance GRCh38 chr20: 61,800,345-63,644,611 , GRCh37.p13 chr20: 60,375,401-62,275,964 STMN3, RPS21, 86 more genes
    nsv6314208copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202 LOC105372698, LOC105372695, 176 more genes
    nsv6134311copy number variation1nstd213human GRCh37 chr20: 59,780,000-61,210,001 , GRCh38.p12 chr20: 61,204,944-62,612,794 LAMA5, PSMA7, 34 more genes
    nsv6134308copy number variation1nstd213human GRCh37 chr20: 55,660,000-60,880,001 , GRCh38.p12 chr20: 57,084,944-62,304,945 TAF4, OSBPL2, 97 more genes
    nsv6134040copy number variation1nstd213human GRCh37 chr20: 51,820,000-60,870,001 , GRCh38.p12 chr20: 53,203,461-62,294,945 MC3R, PPP1R3D, 142 more genes
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