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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 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
    nsv5419601copy number variation1nstd206human GRCh38 chrX: 107,738,368-107,738,711 , GRCh37.p13 chrX: 106,981,598-106,981,941 TSC22D3
    nsv5416445copy number variation1nstd206human GRCh38 chrX: 107,759,023-107,759,130 , GRCh37.p13 chrX: 107,002,253-107,002,360 TSC22D3
    nsv5376853translocation1nstd200human GRCh38 chrX: 107,744,265-107,744,265 , GRCh38 chrX: 107,744,171-107,744,171 , GRCh37.p13 chrX: 106,987,401-106,987,401 , GRCh37.p13 chrX: 106,987,495-106,987,495 TSC22D3
    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
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4779972copy number variation1nstd200human GRCh37 chrX: 106,963,687-106,969,399 , GRCh38.p12 chrX: 107,720,457-107,726,169 TSC22D3
    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
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 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
    nsv4728258copy number variation1nstd102humanUncertain significance GRCh37 chrX: 106,479,615-107,575,960 , GRCh38.p12 chrX: 107,236,385-108,332,730 COL4A6, ATG4A, 16 more genes
    nsv4683721copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,871,849-107,939,618 , GRCh38.p12 chrX: 107,628,619-108,696,388 NCBP2L, TEX13B, 11 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
    nsv4674000copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 105,973,323-110,619,655 , GRCh38.p12 chrX: 106,730,093-111,376,427 CAPN6, COL4A5, 53 more genes
    nsv4636275copy number variation1nstd186human GRCh37 chrX: 106,981,594-106,981,941 , GRCh38.p12 chrX: 107,738,364-107,738,711 TSC22D3
    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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