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Items: 1 to 20 of 228

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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
    nsv7096264copy number variation2nstd102humanUncertain significance GRCh37 chr20: 60,831,241-62,680,869 , GRCh38.p12 chr20: 62,256,185-64,049,516 RPS21, MIR1-1HG, 102 more genes
    nsv7037297copy number variation1nstd229human GRCh38 chr20: 62,355,856-62,434,808 , GRCh37.p13 chr20: 60,930,912-61,009,864 LAMA5, LOC105372709, 6 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
    nsv7033732copy number variation1nstd229human GRCh38 chr20: 62,292,913-62,386,907 , GRCh37.p13 chr20: 60,867,969-60,961,963 ADRM1, LOC105372708, 6 more genes
    nsv7032216copy number variation1nstd229human GRCh38 chr20: 62,357,913-62,396,840 , GRCh37.p13 chr20: 60,932,969-60,971,896 RPS21, LAMA5, 2 more genes
    nsv7028465copy number variation1nstd229human GRCh38 chr20: 62,314,101-62,417,500 , GRCh37.p13 chr20: 60,889,157-60,992,556 CABLES2, RPS21, 6 more genes
    nsv7019693copy number variation1nstd229human GRCh38 chr20: 62,373,801-62,672,900 , GRCh37.p13 chr20: 60,948,857-61,304,252 , GRCh37.p13 chr20|NW_003571063.2: 1-179,899 LOC105372708, RBBP8NL, 16 more genes
    nsv7018443copy number variation1nstd229human GRCh38 chr20: 62,368,777-62,410,618 , GRCh37.p13 chr20: 60,943,833-60,985,674 RBBP8NL, CABLES2, 3 more genes
    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
    nsv6626728copy number variation1nstd224human GRCh37 chr20: 60,921,998-60,976,032 , GRCh38.p12 chr20: 62,346,942-62,400,976 LAMA5, RPS21, 4 more genes
    nsv6626605copy number variation1nstd224human GRCh37 chr20: 60,926,766-60,990,075 , GRCh38.p12 chr20: 62,351,710-62,415,019 LAMA5, RPS21, 5 more genes
    nsv6546982copy number variation1nstd223human GRCh38 chr20: 62,292,913-62,386,907 , GRCh37.p13 chr20: 60,867,969-60,961,963 RPS21, ADRM1, 6 more genes
    nsv6544498copy number variation1nstd223human GRCh38 chr20: 62,383,101-62,385,800 , GRCh37.p13 chr20: 60,958,157-60,960,856 RPS21
    nsv6540791copy number variation1nstd223human GRCh38 chr20: 62,384,062-62,385,369 , GRCh37.p13 chr20: 60,959,118-60,960,425 RPS21
    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
    nsv6134085copy number variation1nstd213human GRCh37 chr20: 60,880,000-61,070,001 , GRCh38.p12 chr20: 62,304,944-62,494,945 LOC105372709, RBBP8NL, 10 more genes
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
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