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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099181copy number variation1nstd231human GRCh38.p12 chr1: 18,899,486-20,046,918 , GRCh37 chr1: 19,225,980-20,373,411 CAPZB, HTR6, 32 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7049927inversion1nstd229human GRCh38 chr1: 12,447,483-21,286,051 , GRCh37.p13 chr1: 12,507,539-21,612,544 SLC25A34, RNA5SP41, 238 more genes
    nsv6646942copy number variation1nstd229human GRCh38 chr1: 19,273,140-19,287,653 , GRCh37.p13 chr1: 19,599,634-19,614,147 AKR7A3, AKR7L
    nsv6646877copy number variation1nstd229human GRCh38 chr1: 19,272,901-19,288,800 , GRCh37.p13 chr1: 19,599,395-19,615,294 AKR7L, AKR7A3
    nsv6646874copy number variation1nstd229human GRCh38 chr1: 19,200,551-19,292,975 , GRCh37.p13 chr1: 19,527,045-19,619,469 AKR7L, EMC1, 5 more genes
    nsv6646791copy number variation1nstd229human GRCh38 chr1: 19,271,401-19,287,700 , GRCh37.p13 chr1: 19,597,895-19,614,194 AKR7L, AKR7A3
    nsv6646589copy number variation1nstd229human GRCh38 chr1: 18,782,901-19,372,400 , GRCh37.p13 chr1: 19,109,395-19,698,894 MIR4695, AKR7A3, 15 more genes
    nsv6646409copy number variation1nstd229human GRCh38 chr1: 19,280,001-19,298,600 , GRCh37.p13 chr1: 19,606,495-19,625,094 LOC100506730, AKR7A3
    nsv6646408copy number variation1nstd229human GRCh38 chr1: 19,271,620-19,280,632 , GRCh37.p13 chr1: 19,598,114-19,607,126 AKR7A3, AKR7L
    nsv6646406copy number variation1nstd229human GRCh38 chr1: 19,221,627-19,301,937 , GRCh37.p13 chr1: 19,548,121-19,628,431 AKR7A3, AKR7A2, 5 more genes
    nsv6334038copy number variation1nstd223human GRCh38 chr1: 19,271,627-19,280,631 , GRCh37.p13 chr1: 19,598,121-19,607,125 AKR7A3, AKR7L
    nsv6317621copy number variation1nstd223human GRCh38 chr1: 19,284,429-19,285,755 , GRCh37.p13 chr1: 19,610,923-19,612,249 AKR7A3
    nsv6290472copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580 MIR1290, RNU6-1099P, 92 more genes
    nsv6138999copy number variation1nstd206human GRCh38 chr1: 19,273,115-19,287,674 , GRCh37.p13 chr1: 19,599,609-19,614,168 AKR7L, AKR7A3
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6133948copy number variation1nstd213human GRCh37 chr1: 17,280,000-26,950,001 , GRCh38.p12 chr1: 16,953,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv6133748copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,960,001 , GRCh38.p12 chr1: 16,943,505-26,633,510 ALPL, C1QA, 250 more genes
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