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Items: 1 to 20 of 333

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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
    nsv5674181copy number variation1nstd102humanPathogenic GRCh37 chrX: 102,508,548-103,080,719 , GRCh38.p12 chrX: 103,253,620-103,825,789 TCEAL1, CNEP1R1P1, 18 more genes
    nsv5673978copy number variation2nstd102humanPathogenic GRCh37 chrX: 103,031,924-103,045,526 , GRCh38.p12 chrX: 103,776,996-103,790,598 PLP1, RAB9B
    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
    nsv4905828copy number variation1nstd200human GRCh38 chrX: 103,740,671-103,956,057 , GRCh37.p13 chrX: 102,995,599-103,118,516 , PLP1, 7 more genes
    nsv4782227copy number variation1nstd200human GRCh37 chrX: 102,995,599-103,210,630 , GRCh38.p12 chrX: 103,740,671-103,956,057 , RNA5SP511, 7 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
    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
    nsv4684131copy number variation1nstd102humanPathogenic GRCh37 chrX: 102,632,399-103,221,016 , GRCh38.p12 chrX: 103,377,471-103,966,443 BEX3, RNA5SP511, 19 more genes
    nsv4684053copy number variation1nstd102humanPathogenic GRCh37 chrX: 103,031,924-103,044,327 , GRCh38.p12 chrX: 103,776,996-103,789,398 RAB9B, PLP1
    nsv4683062copy number variation1nstd102humanPathogenic GRCh37 chrX: 102,831,398-103,220,942 , GRCh38.p12 chrX: 103,576,470-103,966,369 TCEAL4, TMSB15B, 15 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
    nsv4674164copy number variation1nstd102humanPathogenic GRCh37 chrX: 102,742,391-103,109,211 , GRCh38.p12 chrX: 103,487,463-103,854,282 RNA5SP511, RAB40A, 12 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
    nsv4578586copy number variation1nstd102humanPathogenic GRCh37 chrX: 101,029,649-106,702,784 , GRCh38.p12 chrX: 101,774,676-107,459,554 GLRA4, TMSB15B, 115 more genes
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