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Items: 1 to 20 of 299

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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
    nsv7075234inversion1nstd229human GRCh38 chr20: 62,886,537-63,022,704 , GRCh37.p13 chr20: 61,517,889-61,654,056 LINC01749, GID8, 3 more genes
    nsv7064962inversion1nstd229human GRCh38 chr20: 62,710,955-62,963,614 , GRCh37.p13 chr20: 61,342,307-61,594,966 , GID8, 14 more genes
    nsv7064500inversion1nstd229human GRCh38 chr20: 62,961,979-62,994,499 , GRCh37.p13 chr20: 61,593,331-61,625,851 SLC17A9
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7033621copy number variation1nstd229human GRCh38 chr20: 62,954,078-63,070,134 , GRCh37.p13 chr20: 61,585,430-61,701,486 LINC01056, BHLHE23, 4 more genes
    nsv7033339copy number variation1nstd229human GRCh38 chr20: 62,957,087-62,957,127 , GRCh37.p13 chr20: 61,588,439-61,588,479 SLC17A9
    nsv7021890copy number variation1nstd229human GRCh38 chr20: 62,944,201-62,963,600 , GRCh37.p13 chr20: 61,575,553-61,594,952 SLC17A9, GID8
    nsv7021453copy number variation1nstd229human GRCh38 chr20: 62,945,997-63,054,654 , GRCh37.p13 chr20: 61,577,349-61,686,006 GID8, SLC17A9, 5 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
    nsv6626831copy number variation1nstd224human GRCh37 chr20: 61,588,202-61,793,778 , GRCh38.p12 chr20: 62,956,850-63,162,426 LOC105376996, LINC01749, 8 more genes
    nsv6626607copy number variation2nstd224human GRCh37 chr20: 61,588,202-61,599,474 , GRCh38.p12 chr20: 62,956,850-62,968,122 SLC17A9
    nsv6551088copy number variation1nstd223human GRCh38 chr20: 62,943,848-62,973,196 , GRCh37.p13 chr20: 61,575,200-61,604,548 GID8, SLC17A9
    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
    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
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