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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7099302copy number variation6nstd231human GRCh37 chrX: 154,912,942-154,946,932 , GRCh38.p12 chrX: 155,683,281-155,717,271 SPRY3
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7085695copy number variation1nstd229human GRCh38 chrX: 155,686,831-155,687,355 , GRCh37.p13 chrX: 154,916,492-154,917,016 SPRY3
    nsv7085693copy number variation1nstd229human GRCh38 chrX: 155,681,889-155,686,961 , GRCh37.p13 chrX: 154,911,550-154,916,622 SPRY3
    nsv7085692copy number variation1nstd229human GRCh38 chrX: 155,681,700-155,683,294 , GRCh37.p13 chrX: 154,911,361-154,912,955 SPRY3
    nsv7085691copy number variation1nstd229human GRCh38 chrX: 155,679,501-155,692,100 , GRCh37.p13 chrX: 154,909,162-154,921,761 SPRY3
    nsv7085690copy number variation1nstd229human GRCh38 chrX: 155,676,838-155,679,530 , GRCh37.p13 chrX: 154,906,586-154,909,191 SPRY3
    nsv7085689copy number variation1nstd229human GRCh38 chrX: 155,671,011-155,694,295 , GRCh37.p13 chrX: 154,906,586-154,923,956 SPRY3
    nsv7085688copy number variation1nstd229human GRCh38 chrX: 155,668,659-155,683,057 , GRCh37.p13 chrX|NW_003871103.3: 3,102,638-3,110,903 , GRCh37.p13 chrX: 154,898,320-154,906,585 SPRY3
    nsv7085687copy number variation1nstd229human GRCh38 chrX: 155,668,485-155,675,670 , GRCh37.p13 chrX: 154,898,146-154,905,331 , GRCh37.p13 chrX|NW_003871103.3: 3,102,464-3,109,649 SPRY3
    nsv7085686copy number variation1nstd229human GRCh38 chrX: 155,657,174-155,669,014 , GRCh37.p13 chrX|NW_003871103.3: 3,091,153-3,102,993 , GRCh37.p13 chrX: 154,886,835-154,898,675 SPRY3
    nsv7085685copy number variation1nstd229human GRCh38 chrX: 155,652,401-155,663,800 , GRCh37.p13 chrX|NW_003871103.3: 3,086,380-3,097,779 , GRCh37.p13 chrX: 154,882,062-154,893,461 SPRY3
    nsv7085684copy number variation1nstd229human GRCh38 chrX: 155,647,901-155,650,200 , GRCh37.p13 chrX: 154,877,562-154,879,861 , GRCh37.p13 chrX|NW_003871103.3: 3,081,880-3,084,179 SPRY3
    nsv7085683copy number variation1nstd229human GRCh38 chrX: 155,647,001-155,651,300 , GRCh37.p13 chrX|NW_003871103.3: 3,080,980-3,085,279 , GRCh37.p13 chrX: 154,876,662-154,880,961 SPRY3
    nsv7085682copy number variation1nstd229human GRCh38 chrX: 155,646,734-155,651,315 , GRCh37.p13 chrX|NW_003871103.3: 3,080,713-3,085,294 , GRCh37.p13 chrX: 154,876,395-154,880,976 SPRY3
    nsv7085681copy number variation1nstd229human GRCh38 chrX: 155,646,701-155,650,300 , GRCh37.p13 chrX: 154,876,362-154,879,961 , GRCh37.p13 chrX|NW_003871103.3: 3,080,680-3,084,279 SPRY3
    nsv7085680copy number variation1nstd229human GRCh38 chrX: 155,626,001-155,653,800 , GRCh37.p13 chrX: 154,855,662-154,883,461 , GRCh37.p13 chrX|NW_003871103.3: 3,059,980-3,087,779 SPRY3
    nsv7085679copy number variation1nstd229human GRCh38 chrX: 155,618,151-155,622,051 , GRCh37.p13 chrX|NW_003871103.3: 3,052,130-3,056,030 , GRCh37.p13 chrX: 154,847,812-154,851,712 SPRY3
    nsv7085678copy number variation1nstd229human GRCh38 chrX: 155,617,131-155,621,919 , GRCh37.p13 chrX|NW_003871103.3: 3,051,110-3,055,898 , GRCh37.p13 chrX: 154,846,792-154,851,580 SPRY3
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