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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 more genes
    nsv6137735copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,194,251-153,623,000 , GRCh38.p12 chrX: 153,928,798-154,394,658 EMD, MIR3202-1, 20 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5980455copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,884,414-154,363,935 , GRCh37.p13 chrX|NW_003871103.3: 1,318,396-1,797,914 , GRCh37.p13 chrX: 153,149,868-153,592,303 MIR3202-1, FLNA, 23 more genes
    nsv5668728copy number variation1nstd207human GRCh37.p13 chrX|NW_003871103.3: 1,682,677-1,719,794 , GRCh38 chrX: 154,248,698-154,285,815 TEX28, OPN1MW3, 1 more genes
    nsv5564517copy number variation1nstd102humanPathogenic GRCh38 chrX: 153,858,452-154,332,213 , GRCh37.p13 chrX|NW_003871103.3: 1,292,435-1,766,192 , GRCh37.p13 chrX: 153,123,907-153,560,563 OPN1MW2, ARHGAP4, 22 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
    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
    nsv4728292copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,135,257-153,594,096 , GRCh38.p12 chrX: 153,869,802-154,365,728 NAA10, OPN1MW3, 23 more genes
    nsv4728215copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,113,943-153,624,215 , GRCh38.p12 chrX: 153,848,488-154,395,874 ARHGAP4, L1CAM, 24 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
    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
    nsv4674212copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,029,046-153,567,369 , GRCh38.p12 chrX: 153,763,591-154,339,019 TEX28P2, LOC105373386, 29 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
    nsv4633467copy number variation2nstd183human GRCh37 chrX: 153,408,546-153,524,153 , GRCh38.p12 chrX: 154,143,072-154,295,800 TEX28, OPN1MW, 7 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
    nsv4454760copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,990,712-153,650,075 , GRCh38.p12 chrX: 153,725,257-154,421,736 FLNA, ABCD1, 36 more genes
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