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Items: 1 to 20 of 292

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5424382copy number variation1nstd206human GRCh38 chrX: 128,008,251-128,107,757 , GRCh37.p13 chrX: 127,142,230-127,241,736 LOC100129947, ACTRT1
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv4909122copy number variation1nstd200human GRCh38 chrX: 127,930,621-128,515,744 , GRCh37.p13 chrX: 127,064,600-127,649,722 ACTRT1, RUVBL2P1, 6 more genes
    nsv4909120copy number variation1nstd200human GRCh38 chrX: 127,749,422-128,129,267 , GRCh37.p13 chrX: 126,883,403-127,263,245 BTG3P1, LOC100129947, 3 more genes
    nsv4782325copy number variation1nstd200human GRCh37 chrX: 126,883,403-127,263,245 , GRCh38.p12 chrX: 127,749,422-128,129,267 BTG3P1, LOC100129947, 3 more genes
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4765755copy number variation1nstd199human GRCh37 chrX: 127,142,227-127,241,739 , GRCh38.p12 chrX: 128,008,248-128,107,760 LOC100129947, ACTRT1
    nsv4728692copy number variation1nstd102humanPathogenic GRCh37 chrX: 117,120,780-129,850,994 , GRCh38.p12 chrX: 117,986,817-130,717,020 LOC107985709, SLC25A5, 171 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4728493copy number variation1nstd102humanUncertain significance GRCh37 chrX: 126,829,599-127,350,690 , GRCh38.p12 chrX: 127,695,618-128,216,713 BTG3P1, LOC105373333, 4 more genes
    nsv4728439copy number variation1nstd102humanUncertain significance GRCh37 chrX: 126,470,083-127,332,268 , GRCh38.p12 chrX: 127,336,100-128,198,291 LOC105373333, LOC100420320, 6 more genes
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4679893copy number variation1nstd189human GRCh37.p13 chrX: 113,759,648-150,222,670 , GRCh38.p12 chrX: 114,525,195-151,054,198 , AGTR2, 532 more genes
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674403copy number variation1nstd102humanUncertain significance GRCh37 chrX: 126,937,856-128,178,295 , GRCh38.p12 chrX: 127,803,875-129,044,318 LOC107985699, ACTRT1, 10 more genes
    nsv4674080copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,387,417-155,233,731 , GRCh38.p12 chrX: 85,132,411-156,004,066 CSTF2, GPR119, 1029 more genes
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