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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
    nsv5870111copy number variation1nstd209human GRCh38 chrX: 154,414,430-154,414,727 , GRCh37.p13 chrX: 153,642,767-153,643,065 , GRCh37.p13 chrX|NW_003871103.3: 1,848,409-1,848,706 TAFAZZIN
    nsv5674084copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,647,872-153,650,075 , GRCh38.p12 chrX: 154,419,533-154,421,736 TAFAZZIN
    nsv5673981copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,639,844-153,642,537 , GRCh38.p12 chrX: 154,411,508-154,414,200 DNASE1L1, TAFAZZIN
    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
    nsv4787975copy number variation1nstd200human GRCh37 chrX: 153,638,352-153,638,936 , GRCh38.p12 chrX: 154,410,016-154,410,600 DNASE1L1, TAFAZZIN
    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
    nsv4730161inversion20nstd198human GRCh37.p13 chrX: 153,565,303-153,644,627 , GRCh38 chrX: 154,336,953-154,416,288 , GRCh37.p13 chrX|NW_003871103.3: 1,770,932-1,850,267 DNASE1L1, EMD, 5 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
    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
    nsv4683774copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,577,207-153,642,537 , GRCh38.p12 chrX: 154,348,839-154,414,200 DNASE1L1, RPL10, 4 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
    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
    nsv4454892copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 153,640,161-153,649,363 , GRCh38.p12 chrX: 154,411,824-154,421,024 TAFAZZIN, DNASE1L1
    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
    nsv4454214copy number variation1nstd102humanPathogenic GRCh37 chrX: 122,924,044-155,233,731 , GRCh38.p12 chrX: 123,790,194-156,004,066 LOC107985666, FLNA, 555 more genes
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