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Items: 1 to 20 of 269

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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
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5428156copy number variation1nstd206human GRCh37.p13 chrX|NW_004070890.2: 1,517,060-1,518,558 , GRCh38 chrX: 145,992,669-145,994,167 , GRCh37.p13 chrX: 145,074,187-145,075,685 MIR890, MIR888, 1 more genes
    nsv5420852copy number variation1nstd206human GRCh37.p13 chrX|NW_004070890.2: 1,517,569-1,519,132 , GRCh38 chrX: 145,993,178-145,994,741 , GRCh37.p13 chrX: 145,074,696-145,076,259 MIR890, MIR888, 2 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
    nsv4894126copy number variation1nstd200human GRCh38 chrX: 145,993,248-145,994,671 , GRCh37.p13 chrX: 145,074,766-145,076,189 , GRCh37.p13 chrX|NW_004070890.2: 1,517,639-1,519,062 MIR892C, MIR890, 2 more genes
    nsv4894124copy number variation1nstd200human GRCh38 chrX: 145,966,984-145,998,766 , GRCh37.p13 chrX|NW_004070890.2: 1,491,375-1,523,157 , GRCh37.p13 chrX: 145,048,502-145,080,284 MIR890, MIR888, 3 more genes
    nsv4787812copy number variation1nstd200human GRCh37 chrX: 145,074,767-145,076,176 , GRCh38.p12 chrX: 145,993,249-145,994,658 MIR892C, MIR890, 1 more genes
    nsv4787811copy number variation1nstd200human GRCh37 chrX: 145,074,160-145,075,715 , GRCh38.p12 chrX: 145,992,642-145,994,197 MIR892C, MIR888, 1 more genes
    nsv4787809copy number variation1nstd200human GRCh37 chrX: 145,048,502-145,080,284 , GRCh38.p12 chrX: 145,966,984-145,998,766 MIR892A, MIR892B, 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
    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
    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
    nsv4517626copy number variation1nstd166human GRCh37.p13 chrX: 145,074,759-145,076,175 , GRCh38.p12 chrX: 145,993,241-145,994,657 MIR890, MIR888, 1 more genes
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