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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137164copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 85,166,265-85,166,342 , GRCh38 chrX: 85,911,260-85,911,337 CHM
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098680copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,282,475-85,302,634 , GRCh38.p12 chrX: 86,027,471-86,047,630 CHM
    nsv7098679copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,233,751-85,233,915 , GRCh38.p12 chrX: 85,978,747-85,978,911 CHM
    nsv7098678copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,119,635-85,128,237 , GRCh38.p12 chrX: 85,864,630-85,873,232 CHM
    nsv7098577copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,282,475-85,282,581 , GRCh38.p12 chrX: 86,027,471-86,027,577 CHM
    nsv7098576copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,212,840-85,214,002 , GRCh38.p12 chrX: 85,957,835-85,958,997 CHM
    nsv7098575copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,149,173-85,166,363 , GRCh38.p12 chrX: 85,894,168-85,911,358 CHM, MIR361
    nsv7098574copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,119,635-85,156,213 , GRCh38.p12 chrX: 85,864,630-85,901,208 CHM
    nsv7098573copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,119,625-85,119,836 , GRCh38.p12 chrX: 85,864,620-85,864,831 CHM
    nsv7098556copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,233,751-85,302,644 , GRCh38.p12 chrX: 85,978,747-86,047,640 CHM
    nsv7098555copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 85,218,687-85,221,623 , GRCh38.p12 chrX: 85,963,682-85,966,618 CHM
    nsv7098554copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,223,644 , GRCh38.p12 chrX: 85,864,630-85,968,639 CHM, MIR361
    nsv7098553copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,149,309 , GRCh38.p12 chrX: 85,864,630-85,894,304 CHM
    nsv7098338copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,218,650-85,223,644 , GRCh38.p12 chrX: 85,963,645-85,968,639 CHM
    nsv7098337copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,119,635-85,302,644 , GRCh38.p12 chrX: 85,864,630-86,047,640 MIR361, CHM
    nsv7098336copy number variation1nstd102humanUncertain significance GRCh37 chrX: 84,600,846-85,302,644 , GRCh38.p12 chrX: 85,345,840-86,047,640 CHM, SFR1P2, 3 more genes
    nsv7090117copy number variation1nstd229human GRCh38 chrX: 86,042,663-86,042,835 , GRCh37.p13 chrX: 85,297,667-85,297,839 CHM
    nsv7090116copy number variation1nstd229human GRCh38 chrX: 86,018,401-86,025,300 , GRCh37.p13 chrX: 85,273,405-85,280,304 CHM
    nsv7090115copy number variation1nstd229human GRCh38 chrX: 85,996,951-85,997,294 , GRCh37.p13 chrX: 85,251,955-85,252,298 CHM
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