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Items: 1 to 20 of 1483

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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
    nsv7143061copy number variation1nstd232human GRCh37.p13 chrX: 6,720,980-6,721,100 , GRCh38.p12 chrX: 6,802,939-6,803,059 PUDP
    nsv7140148copy number variation1nstd232human GRCh37.p13 chrX: 6,720,985-6,721,100 , GRCh38.p12 chrX: 6,802,944-6,803,059 PUDP
    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
    nsv7077650copy number variation1nstd229human GRCh38 chrX: 6,898,599-6,899,343 , GRCh37.p13 chrX: 6,816,640-6,817,384 PUDP
    nsv7077603copy number variation1nstd229human GRCh38 chrX: 6,896,401-6,899,300 , GRCh37.p13 chrX: 6,814,442-6,817,341 PUDP
    nsv7077564copy number variation1nstd229human GRCh38 chrX: 6,915,152-6,945,067 , GRCh37.p13 chrX: 6,833,193-6,863,108 PUDP
    nsv7077185copy number variation1nstd229human GRCh38 chrX: 7,003,101-7,018,600 , GRCh37.p13 chrX: 6,921,142-6,936,641 PUDP, LOC107987331
    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
    nsv7076275copy number variation1nstd229human GRCh38 chrX: 6,943,518-6,958,664 , GRCh37.p13 chrX: 6,861,559-6,876,705 PUDP
    nsv7076173copy number variation1nstd229human GRCh38 chrX: 6,218,213-6,874,209 , GRCh37.p13 chrX: 6,136,254-6,792,250 LOC105373156, NLGN4X, 4 more genes
    nsv7076134copy number variation1nstd229human GRCh38 chrX: 6,788,101-6,797,800 , GRCh37.p13 chrX: 6,706,142-6,715,841 PUDP
    nsv7075267copy number variation1nstd229human GRCh38 chrX: 6,793,601-7,019,700 , GRCh37.p13 chrX: 6,711,642-6,937,741 RPS27AP17, PUDP, 1 more genes
    nsv7075237copy number variation1nstd229human GRCh38 chrX: 6,779,760-6,784,333 , GRCh37.p13 chrX: 6,697,801-6,702,374 PUDP
    nsv7075072copy number variation1nstd229human GRCh38 chrX: 6,838,601-6,841,600 , GRCh37.p13 chrX: 6,756,642-6,759,641 PUDP
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