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Items: 1 to 20 of 1098

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148045copy number variation1nstd102humanPathogenic GRCh38 chrX: 7,050,240-7,350,316 , GRCh37.p13 chrX: 6,968,281-7,268,357 MIR4767, PUDP, 1 more genes
    nsv7137077copy number variation1nstd102humanPathogenic GRCh37 chrX: 6,968,337-8,434,424 , GRCh38.p12 chrX: 7,050,296-8,466,383 PUDP, PNPLA4, 8 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098871copy number variation1nstd102humanPathogenic GRCh37 chrX: 6,451,786-7,894,160 , GRCh38.p12 chrX: 6,533,745-7,926,119 STS, PUDP, 7 more genes
    nsv7098545copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 7,171,217-7,177,833 , GRCh38.p12 chrX: 7,253,176-7,259,792 STS
    nsv7098328copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,223,067-7,268,302 , GRCh38.p12 chrX: 7,305,026-7,350,261 STS
    nsv7077945copy number variation1nstd229human GRCh38 chrX: 7,199,501-7,202,200 , GRCh37.p13 chrX: 7,117,542-7,120,241 STS
    nsv7077296copy number variation1nstd229human GRCh38 chrX: 7,296,288-7,476,129 , GRCh37.p13 chrX: 7,214,329-7,394,170 STS
    nsv7077116copy number variation1nstd229human GRCh38 chrX: 6,946,057-7,319,872 , GRCh37.p13 chrX: 6,864,098-7,237,913 LOC107987331, PUDP, 3 more genes
    nsv7077061copy number variation1nstd229human GRCh38 chrX: 6,945,408-7,250,900 , GRCh37.p13 chrX: 6,863,449-7,168,941 MIR4767, RPS27AP17, 3 more genes
    nsv7076928copy number variation1nstd229human GRCh38 chrX: 7,160,091-7,687,337 , GRCh37.p13 chrX: 7,078,132-7,605,378 STS
    nsv7076852copy number variation1nstd229human GRCh38 chrX: 7,134,242-7,198,567 , GRCh37.p13 chrX: 7,052,283-7,116,608 MIR4767, STS, 1 more genes
    nsv7076823copy number variation1nstd229human GRCh38 chrX: 7,281,582-7,357,292 , GRCh37.p13 chrX: 7,199,623-7,275,333 STS
    nsv7076594copy number variation1nstd229human GRCh38 chrX: 6,571,311-7,300,414 , GRCh37.p13 chrX: 6,489,352-7,218,455 PUDP, LOC107987331, 3 more genes
    nsv7076183copy number variation1nstd229human GRCh38 chrX: 7,203,773-7,215,059 , GRCh37.p13 chrX: 7,121,814-7,133,100 STS
    nsv7074750copy number variation1nstd229human GRCh38 chrX: 6,540,406-7,984,374 , GRCh37.p13 chrX: 6,458,447-7,952,415 PNPLA4, STS, 6 more genes
    nsv7074595copy number variation1nstd229human GRCh38 chrX: 6,865,523-7,881,779 , GRCh37.p13 chrX: 6,783,564-7,849,820 RPS27AP17, MIR4767, 4 more genes
    nsv7074594copy number variation1nstd229human GRCh38 chrX: 6,711,976-7,409,585 , GRCh37.p13 chrX: 6,630,017-7,327,626 MIR4767, RPS27AP17, 3 more genes
    nsv7074005copy number variation1nstd229human GRCh38 chrX: 7,300,799-7,378,574 , GRCh37.p13 chrX: 7,218,840-7,296,615 STS
    nsv7073600copy number variation1nstd229human GRCh38 chrX: 6,965,701-7,683,300 , GRCh37.p13 chrX: 6,883,742-7,601,341 LOC107987331, MIR4767, 3 more genes
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