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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
    nsv5878163copy number variation1nstd209human GRCh38 chrX: 131,348,092-131,861,518 , GRCh37.p13 chrX: 130,482,066-130,995,546 HDGFP1, OR1AA1P, 12 more genes
    nsv5414094copy number variation1nstd206human GRCh38 chrX: 131,334,000-131,840,381 , GRCh37.p13 chrX: 130,467,974-130,974,409 LOC102723546, OR13H1, 13 more genes
    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
    nsv4909143copy number variation1nstd200human GRCh38 chrX: 131,518,601-131,935,134 , GRCh37.p13 chrX: 130,652,575-131,069,162 OR2AF1P, FIRRE, 6 more genes
    nsv4909142copy number variation1nstd200human GRCh38 chrX: 131,512,551-131,811,922 , GRCh37.p13 chrX: 130,646,525-130,945,950 OR2AF1P, FIRRE, 6 more genes
    nsv4909140copy number variation1nstd200human GRCh38 chrX: 131,469,391-131,995,434 , GRCh37.p13 chrX: 130,603,365-131,129,462 FIRRE, NLRP7P1, 8 more genes
    nsv4909138copy number variation1nstd200human GRCh38 chrX: 131,154,720-131,587,047 , GRCh37.p13 chrX: 130,288,694-130,721,021 LOC100421910, OR11Q1P, 10 more genes
    nsv4782340copy number variation1nstd200human GRCh37 chrX: 130,646,525-130,945,950 , GRCh38.p12 chrX: 131,512,551-131,811,922 OR7L1P, HDGFP1, 6 more genes
    nsv4782339copy number variation1nstd200human GRCh37 chrX: 130,603,365-131,129,462 , GRCh38.p12 chrX: 131,469,391-131,995,434 RNA5SP514, OR7L1P, 8 more genes
    nsv4782338copy number variation1nstd200human GRCh37 chrX: 130,288,694-130,721,021 , GRCh38.p12 chrX: 131,154,720-131,587,047 LOC107985705, OR1AA1P, 10 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
    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
    nsv4728178copy number variation1nstd102humanUncertain significance GRCh37 chrX: 130,483,014-131,224,642 , GRCh38.p12 chrX: 131,349,040-132,090,614 OR2AF1P, MCRIP2P1, 15 more genes
    nsv4728168copy number variation1nstd102humanLikely benign GRCh37 chrX: 130,615,694-131,152,624 , GRCh38.p12 chrX: 131,481,720-132,018,596 PNKDP1, OR13H1, 8 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
    nsv4679253copy number variation1nstd189human GRCh37.p13 chrX: 130,435,797-130,974,750 , GRCh38.p12 chrX: 131,301,823-131,840,722 OR1AA1P, OR2AF1P, 14 more genes
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