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Items: 1 to 20 of 157

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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
    nsv7148178copy number variation1nstd102humanPathogenic GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157 GID8, TCFL5, 60 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
    nsv7095910copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,471,874-62,078,210 , GRCh38.p12 chr20: 62,840,522-63,446,857 LINC01749, HAR1A, 32 more genes
    nsv7061289inversion1nstd229human GRCh38 chr20: 63,026,492-64,008,482 , GRCh37.p13 chr20: 61,657,844-62,639,835 TNFRSF6B, MIR941-5, 60 more genes
    nsv7059476inversion1nstd229human GRCh38 chr20: 63,024,183-64,005,567 , GRCh37.p13 chr20: 61,655,535-62,636,920 RTEL1-TNFRSF6B, LOC105372721, 60 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
    nsv7028570copy number variation1nstd229human GRCh38 chr20: 63,175,001-63,178,000 , GRCh37.p13 chr20: 61,806,353-61,809,352 MIR124-3
    nsv7020672copy number variation1nstd229human GRCh38 chr20: 63,054,489-63,176,967 , GRCh37.p13 chr20: 61,685,841-61,808,319 MIR124-3, LOC105376996, 4 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
    nsv6550576copy number variation1nstd223human GRCh38 chr20: 63,167,470-63,198,883 , GRCh37.p13 chr20: 61,798,822-61,830,235 YTHDF1, MIR124-3
    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
    nsv6315031copy number variation1nstd102humanUncertain significance GRCh38 chr20: 62,941,782-63,658,260 , GRCh37.p13 chr20: 61,573,134-62,289,613 GMEB2, LOC105372724, 38 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
    nsv6314138copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,797,521-62,318,983 , GRCh38.p12 chr20: 63,166,169-63,687,630 HELZ2, MIR124-3, 27 more genes
    nsv6314131copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202 HAR1A, PPDPF, 100 more genes
    nsv6314091copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202 TPD52L2, MIR941-5, 72 more genes
    nsv6311089copy number variation2nstd102humanUncertain significance GRCh37 chr20: 61,448,417-62,124,660 , GRCh38.p12 chr20: 62,817,065-63,493,307 ARFGAP1, LOC105376996, 33 more genes
    nsv6291816copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,634,256-61,975,378 , GRCh38.p12 chr20: 63,002,904-63,344,026 BIRC7, ARFGAP1, 18 more genes
    nsv6291738copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202 PTK6, C20orf204, 63 more genes
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