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Items: 1 to 20 of 327

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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
    nsv5727535mobile element insertion1nstd211human GRCh38 chrX: 134,888,171-134,888,171 , GRCh37.p13 chrX: 134,022,201-134,022,201 MOSPD1
    nsv5727088mobile element insertion1nstd211human GRCh38 chrX: 134,896,762-134,896,762 , GRCh37.p13 chrX: 134,030,792-134,030,792 MOSPD1
    nsv5554698mobile element insertion1nstd206human GRCh38 chrX: 134,896,762-134,896,813 , GRCh37.p13 chrX: 134,030,792-134,030,843 MOSPD1
    nsv5365494translocation1nstd200human GRCh38 chrX: 134,888,171-134,888,171 , GRCh38 chr16: 5,203,820-5,203,820 , GRCh37.p13 chr16: 5,253,821-5,253,821 , GRCh37.p13 chrX: 134,022,201-134,022,201 LOC105371067, MOSPD1
    nsv5196684mobile element insertion1nstd203human GRCh38 chrX: 134,896,753-134,896,762 , GRCh37.p13 chrX: 134,030,783-134,030,792 MOSPD1
    nsv5189853mobile element insertion1nstd203human GRCh38 chrX: 134,888,158-134,888,171 , GRCh37.p13 chrX: 134,022,188-134,022,201 MOSPD1
    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
    nsv4872403mobile element deletion1nstd200human GRCh37 chrX: 134,035,397-134,035,684 , GRCh38.p12 chrX: 134,901,367-134,901,654 MOSPD1
    nsv4780494copy number variation1nstd200human GRCh37 chrX: 134,038,715-134,041,055 , GRCh38.p12 chrX: 134,904,685-134,907,025 MOSPD1
    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
    nsv4728667copy number variation1nstd102humanUncertain significance GRCh37 chrX: 132,268,495-134,235,471 , GRCh38.p12 chrX: 133,134,467-135,101,441 RNU4-44P, MIR19B2, 44 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
    nsv4728326copy number variation1nstd102humanUncertain significance GRCh37 chrX: 133,771,926-134,162,280 , GRCh38.p12 chrX: 134,637,896-135,028,250 PLAC1, MOSPD1, 9 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
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