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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
    nsv7147673insertion1nstd232human GRCh37.p13 chr20: 61,992,783-61,992,783 , GRCh38.p12 chr20: 63,361,431-63,361,431 CHRNA4, LOC100130587
    nsv7146688copy number variation1nstd232human GRCh37.p13 chr20: 61,988,489-61,988,566 , GRCh38.p12 chr20: 63,357,137-63,357,214 CHRNA4
    nsv7137319insertion1nstd232human GRCh37.p13 chr20: 61,996,150-61,996,150 , GRCh38.p12 chr20: 63,364,798-63,364,798 CHRNA4, LOC100130587
    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
    nsv7096082copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr20: 61,978,090-62,324,656 , GRCh38.p12 chr20: 63,346,738-63,693,303 SRMS, KCNQ2, 17 more genes
    nsv7096081copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,978,090-62,076,207 , GRCh38.p12 chr20: 63,346,738-63,444,854 CHRNA4, KCNQ2, 3 more genes
    nsv7095911copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,978,090-62,039,909 , GRCh38.p12 chr20: 63,346,738-63,408,556 LOC100130587, KCNQ2, 1 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
    nsv7095801copy number variation1nstd102humanUncertain significance GRCh37 chr20: 61,978,090-62,059,808 , GRCh38.p12 chr20: 63,346,738-63,428,455 LOC100130587, KCNQ2, 2 more genes
    nsv7068946inversion1nstd229human GRCh38 chr20: 63,354,807-63,354,887 , GRCh37.p13 chr20: 61,986,159-61,986,239 CHRNA4
    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
    nsv7037261copy number variation1nstd229human GRCh38 chr20: 63,343,399-63,345,062 , GRCh37.p13 chr20: 61,974,751-61,976,414 CHRNA4
    nsv7037078copy number variation1nstd229human GRCh38 chr20: 54,988,450-63,850,628 , GRCh37.p13 chr20: 53,604,989-62,481,981 , RPL39P, 209 more genes
    nsv7036284copy number variation1nstd229human GRCh38 chr20: 63,311,982-63,349,320 , GRCh37.p13 chr20: 61,943,334-61,980,672 COL20A1, CHRNA4, 1 more genes
    nsv7033903copy number variation1nstd229human GRCh38 chr20: 63,373,278-63,391,663 , GRCh37.p13 chr20: 62,004,630-62,023,016 CHRNA4
    nsv7033448copy number variation1nstd229human GRCh38 chr20: 63,346,694-63,346,897 , GRCh37.p13 chr20: 61,978,046-61,978,249 CHRNA4
    nsv7031003copy number variation1nstd229human GRCh38 chr20: 63,305,401-63,492,900 , GRCh37.p13 chr20: 61,936,753-62,124,253 RNU6-994P, LOC105372724, 7 more genes
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