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Items: 1 to 20 of 124

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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
    nsv6646878copy number variation1nstd229human GRCh38 chr1: 19,306,007-19,314,296 , GRCh37.p13 chr1: 19,632,501-19,640,790 SLC66A1, AKR7A2
    nsv6646792copy number variation1nstd229human GRCh38 chr1: 19,296,068-19,306,205 , GRCh37.p13 chr1: 19,622,562-19,632,699 LOC100506730, RNU6-1099P, 1 more genes
    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
    nsv6646411copy number variation1nstd229human GRCh38 chr1: 19,299,801-19,321,500 , GRCh37.p13 chr1: 19,626,295-19,647,994 RNU6-1099P, AKR7A2, 1 more genes
    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
    nsv6625945copy number variation1nstd224human GRCh37 chr1: 19,627,931-19,650,220 , GRCh38.p12 chr1: 19,301,437-19,323,726 RNU6-1099P, SLC66A1, 1 more genes
    nsv6318183copy number variation1nstd223human GRCh38 chr1: 19,290,651-19,321,474 , GRCh37.p13 chr1: 19,617,145-19,647,968 LOC100506730, SLC66A1, 2 more genes
    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
    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
    nsv6133609copy number variation1nstd213human GRCh37 chr1: 18,830,000-19,700,001 , GRCh38.p12 chr1: 18,503,506-19,373,507 CAPZB, PAX7, 17 more genes
    nsv6133572copy number variation1nstd213human GRCh37 chr1: 17,270,000-26,950,001 , GRCh38.p12 chr1: 16,943,505-26,623,510 ALPL, C1QA, 250 more genes
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5068863mobile element insertion1nstd203human GRCh38 chr1: 19,306,444-19,306,451 , GRCh37.p13 chr1: 19,632,938-19,632,945 AKR7A2
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