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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
    nsv5560505sequence alteration1nstd206human GRCh37.p13 chrX|NW_004070887.1: 28,674-354,321 , GRCh38 chrX: 135,097,530-135,423,178 , GRCh37.p13 chrX: 134,231,560-134,557,103 SMIM10L2A, LOC100419794, 14 more genes
    nsv5421213copy number variation1nstd206human GRCh38 chrX: 135,131,190-135,811,381 , GRCh37.p13 chrX: 134,265,118-134,927,793 , GRCh37.p13 chrX|NW_004070887.1: 62,334-742,524 SAGE2P, LOC650024, 27 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
    nsv4909162copy number variation1nstd200human GRCh38 chrX: 135,397,075-135,455,721 , GRCh37.p13 chrX|NW_004070887.1: 328,218-386,864 , GRCh37.p13 chrX: 134,531,000-134,589,646 LOC100506790, RNA5SP515, 2 more genes
    nsv4909160copy number variation1nstd200human GRCh38 chrX: 134,991,237-135,433,391 , GRCh37.p13 chrX: 134,202,887-134,567,316 , GRCh37.p13 chrX|NW_004070887.1: 1-364,534 , ETDA, 22 more genes
    nsv4782355copy number variation1nstd200human GRCh37 chrX: 134,531,000-134,589,646 , GRCh38.p12 chrX: 135,397,075-135,455,721 CROCCP1, LOC100506790, 2 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
    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
    nsv4684082copy number variation1nstd102humanUncertain significance GRCh37 chrX: 134,314,878-134,797,939 , GRCh38.p12 chrX: 135,180,954-135,664,224 SAGE4P, LOC105373342, 17 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
    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
    nsv4578241copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,757,437-155,208,244 , GRCh38.p12 chrX: 123,623,586-155,978,579 ABCD1, AMD1P2, 557 more genes
    nsv4516714copy number variation1nstd166human GRCh37.p13 chrX: 134,499,299-134,929,000 , GRCh38.p12 chrX: 135,365,374-135,795,008 WDR4P1, SAGE4P, 15 more genes
    nsv4454214copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,924,044-155,233,731 , GRCh38.p12 chrX: 123,790,194-156,004,066 LOC107985666, FLNA, 555 more genes
    nsv4452492copy number variation1nstd102humanPathogenic GRCh37 chrX: 58,455,352-155,233,731 , GRCh38.p12 chrX: 58,428,919-156,004,066 RNU6-122P, LOC100421910, 1347 more genes
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