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Items: 1 to 20 of 308

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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
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5876063copy number variation1nstd209human GRCh38 chrX: 154,459,875-154,459,946 , GRCh37.p13 chrX: 153,688,215-153,688,286 , GRCh37.p13 chrX|NW_003871103.3: 1,893,854-1,893,925 PLXNA3
    nsv5871292copy number variation1nstd209human GRCh38 chrX: 154,460,911-154,460,972 , GRCh37.p13 chrX: 153,689,251-153,689,312 , GRCh37.p13 chrX|NW_003871103.3: 1,894,890-1,894,951 PLXNA3
    nsv5422430copy number variation1nstd206human GRCh38 chrX: 154,461,797-154,462,021 , GRCh37.p13 chrX|NW_003871103.3: 1,895,776-1,896,000 , GRCh37.p13 chrX: 153,690,137-153,690,361 PLXNA3
    nsv5416970copy number variation1nstd206human GRCh38 chrX: 154,460,917-154,460,973 , GRCh37.p13 chrX: 153,689,257-153,689,313 , GRCh37.p13 chrX|NW_003871103.3: 1,894,896-1,894,952 PLXNA3
    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
    nsv4909290copy number variation1nstd200human GRCh38 chrX: 154,456,146-154,457,141 , GRCh37.p13 chrX|NW_003871103.3: 1,890,125-1,891,120 , GRCh37.p13 chrX: 153,684,493-153,685,481 PLXNA3
    nsv4787980copy number variation1nstd200human GRCh37 chrX: 153,690,235-153,690,327 , GRCh38.p12 chrX: 154,461,895-154,461,987 PLXNA3
    nsv4787979copy number variation1nstd200human GRCh37 chrX: 153,688,195-153,688,319 , GRCh38.p12 chrX: 154,459,855-154,459,979 PLXNA3
    nsv4787978copy number variation1nstd200human GRCh37 chrX: 153,687,626-153,689,784 , GRCh38.p12 chrX: 154,459,286-154,461,444 PLXNA3
    nsv4787977copy number variation1nstd200human GRCh37 chrX: 153,686,612-153,686,730 , GRCh38.p12 chrX: 154,458,272-154,458,390 PLXNA3
    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
    nsv4752074copy number variation1nstd199human GRCh37 chrX: 153,689,255-153,689,317 , GRCh38.p12 chrX: 154,460,915-154,460,977 PLXNA3
    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
    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
    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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