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Items: 1 to 20 of 253

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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
    nsv7138163copy number variation1nstd232human GRCh37.p13 chr20: 61,676,577-61,676,655 , GRCh38.p12 chr20: 63,045,225-63,045,303 LINC01749, LINC01056
    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
    nsv7036132copy number variation1nstd229human GRCh38 chr20: 63,035,201-63,047,000 , GRCh37.p13 chr20: 61,666,553-61,678,352 LINC01749, LINC00029, 1 more genes
    nsv7035502copy number variation1nstd229human GRCh38 chr20: 62,999,313-63,140,948 , GRCh37.p13 chr20: 61,630,665-61,772,300 BHLHE23, HAR1B, 7 more genes
    nsv7034362copy number variation1nstd229human GRCh38 chr20: 63,044,336-63,053,889 , GRCh37.p13 chr20: 61,675,688-61,685,241 LINC01056, LINC01749
    nsv7033662copy number variation1nstd229human GRCh38 chr20: 63,034,909-63,045,789 , GRCh37.p13 chr20: 61,666,261-61,677,141 LINC00029, LINC01749, 1 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
    nsv7030826copy number variation1nstd229human GRCh38 chr20: 63,018,201-63,076,100 , GRCh37.p13 chr20: 61,649,553-61,707,452 LINC01749, LINC00029, 2 more genes
    nsv7030059copy number variation1nstd229human GRCh38 chr20: 62,991,335-63,050,687 , GRCh37.p13 chr20: 61,622,687-61,682,039 LINC00029, LINC01749, 3 more genes
    nsv7029969copy number variation1nstd229human GRCh38 chr20: 63,036,900-63,040,007 , GRCh37.p13 chr20: 61,668,252-61,671,359 LINC01749, LINC00029, 1 more genes
    nsv7023389copy number variation1nstd229human GRCh38 chr20: 63,048,785-63,049,740 , GRCh37.p13 chr20: 61,680,137-61,681,092 LINC01749, LINC01056
    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
    nsv7019317copy number variation1nstd229human GRCh38 chr20: 63,035,125-63,045,795 , GRCh37.p13 chr20: 61,666,477-61,677,147 LINC00029, LINC01749, 1 more genes
    nsv7018842copy number variation1nstd229human GRCh38 chr20: 62,995,087-63,118,851 , GRCh37.p13 chr20: 61,626,439-61,750,203 HAR1A, LINC01749, 6 more genes
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