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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
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5376532translocation1nstd200human GRCh38 chrX: 77,652,067-77,652,067 , GRCh38 chrX: 77,451,027-77,451,027 , GRCh37.p13 chrX|NW_003871101.3: 8,289-8,289 , GRCh37.p13 chrX|NW_003871101.3: 209,329-209,329 , GRCh37.p13 chrX: 76,907,557-76,907,557 , GRCh37.p13 chrX: 76,706,518-76,706,518 FGF16, ATRX
    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
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 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
    nsv4728229copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,131,829-77,015,522 , GRCh38.p12 chrX: 76,911,404-77,760,041 MIR325, FGF16, 7 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4674722copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,707,749-77,398,963 , GRCh38.p12 chrX: 77,452,258-78,143,466 FGF16, COX7B, 10 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
    nsv4451868copy number variation1nstd102humanPathogenic GRCh37 chrX: 74,667,077-90,312,981 , GRCh38.p12 chrX: 75,447,242-91,057,982 ZDHHC15, POU3F4, 120 more genes
    nsv4451334copy number variation1nstd102humanUncertain significance GRCh37 chrX: 76,205,499-76,982,189 , GRCh38.p12 chrX: 76,985,074-77,726,712 MIR325, RNA5SP509, 6 more genes
    nsv4450820copy number variation1nstd102humanPathogenic GRCh37 chrX: 40,572,613-92,796,528 , GRCh38.p12 chrX: 40,713,361-93,541,529 HNRNPA1P25, MPV17L2P1, 755 more genes
    nsv4450523copy number variation1nstd102humanUncertain significance GRCh37 chrX: 54,941,868-155,233,731 , GRCh38.p12 chrX: 54,915,435-156,004,066 LOC105373348, MIR548AN, 1396 more genes
    nsv4380296copy number variation3nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , RPL31P63, 2192 more genes
    nsv4367211copy number variation1nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , MIR421, 2192 more genes
    nsv4366599copy number variation1nstd173human GRCh37 chrX: 32,881,264-91,902,765 , GRCh38.p12 chrX: 32,863,147-92,647,766 , OTC, 843 more genes
    nsv4354951copy number variation1nstd102humanPathogenic GRCh37 chrX: 15,323,210-153,542,100 , GRCh38.p12 chrX: 15,305,088-154,313,750 OR5BH1P, H2BP8, 1929 more genes
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