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Items: 1 to 20 of 722

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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
    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
    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
    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
    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
    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
    nsv7073565copy number variation1nstd229human GRCh38 chrX: 6,796,870-7,812,467 , GRCh37.p13 chrX: 6,714,911-7,780,508 PUDP, LOC107987331, 3 more genes
    nsv7073495copy number variation1nstd229human GRCh38 chrX: 7,130,824-7,339,232 , GRCh37.p13 chrX: 7,048,865-7,257,273 MIR4767, PUDP, 1 more genes
    nsv7071565copy number variation1nstd229human GRCh38 chrX: 6,680,562-7,267,104 , GRCh37.p13 chrX: 6,598,603-7,185,145 MIR4767, PUDP, 3 more genes
    nsv7070766copy number variation1nstd229human GRCh38 chrX: 7,123,120-7,210,780 , GRCh37.p13 chrX: 7,041,161-7,128,821 STS, PUDP, 1 more genes
    nsv7070615copy number variation1nstd229human GRCh38 chrX: 7,062,027-7,785,991 , GRCh37.p13 chrX: 6,980,068-7,754,032 MIR4767, PUDP, 1 more genes
    nsv7070420copy number variation1nstd229human GRCh38 chrX: 7,087,794-7,352,148 , GRCh37.p13 chrX: 7,005,835-7,270,189 MIR4767, PUDP, 1 more genes
    nsv7069229copy number variation1nstd229human GRCh38 chrX: 6,884,719-7,205,377 , GRCh37.p13 chrX: 6,802,760-7,123,418 MIR4767, LOC107987331, 3 more genes
    nsv7068825copy number variation1nstd229human GRCh38 chrX: 6,577,192-8,071,531 , GRCh37.p13 chrX: 6,495,233-8,039,572 PNPLA4, STS, 6 more genes
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