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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6975585copy number variation1nstd229human GRCh38 chr15: 43,624,353-43,787,662 , GRCh37.p13 chr15: 43,916,551-44,079,860 RNU6-610P, ELL3, 11 more genes
    nsv6975170copy number variation1nstd229human GRCh38 chr15: 43,479,701-43,751,300 , GRCh37.p13 chr15: 43,771,899-44,043,498 CKMT1B, PPIP5K1P1-CATSPER2, 15 more genes
    nsv6971514copy number variation1nstd229human GRCh38 chr15: 43,760,926-43,883,619 , GRCh37.p13 chr15: 44,053,124-44,175,817 PDIA3, SERF2-C15ORF63, 9 more genes
    nsv6966735copy number variation1nstd229human GRCh38 chr15: 43,770,070-43,771,124 , GRCh37.p13 chr15: 44,062,268-44,063,322 PDIA3, ELL3
    nsv6623114copy number variation3nstd224human GRCh37 chr15: 43,924,420-44,038,850 , GRCh38.p12 chr15: 43,632,222-43,746,652 CKMT1A, STRCP1, 9 more genes
    nsv6593866inversion1nstd223human GRCh38 chr15: 43,760,531-43,760,979 , GRCh37.p13 chr15: 44,052,729-44,053,177 PDIA3
    nsv6585806inversion1nstd223human GRCh38 chr15: 43,749,007-43,749,584 , GRCh37.p13 chr15: 44,041,205-44,041,782 PDIA3
    nsv6583884inversion1nstd223human GRCh38 chr15: 43,760,114-43,760,639 , GRCh37.p13 chr15: 44,052,312-44,052,837 PDIA3
    nsv6580542inversion1nstd223human GRCh38 chr15: 43,748,374-43,748,918 , GRCh37.p13 chr15: 44,040,572-44,041,116 PDIA3
    nsv6507995copy number variation1nstd223human GRCh38 chr15: 43,748,305-43,749,532 , GRCh37.p13 chr15: 44,040,503-44,041,730 PDIA3
    nsv6497704copy number variation1nstd223human GRCh38 chr15: 43,757,301-43,761,100 , GRCh37.p13 chr15: 44,049,499-44,053,298 PDIA3
    nsv6291560copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,215,243-44,632,384 , GRCh38.p12 chr15: 42,923,045-44,340,186 PPIP5K1P1-CATSPER2, STRCP1, 44 more genes
    nsv6290201copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,851,199-44,038,820 , GRCh38.p12 chr15: 43,559,001-43,746,622 CATSPER2P1, CKMT1A, 13 more genes
    nsv6290131copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chr15: 43,851,199-44,038,794 , GRCh38.p12 chr15: 43,559,001-43,746,596 STRCP1, CKMT1B, 13 more genes
    nsv5600432copy number variation1nstd207human GRCh38 chr15: 43,747,391-43,747,745 , GRCh37.p13 chr15: 44,039,589-44,039,943 PDIA3
    nsv5597957copy number variation1nstd207human GRCh38 chr15: 43,745,472-43,745,779 , GRCh37.p13 chr15: 44,037,670-44,037,977 CATSPER2P1, PDIA3
    nsv5512663copy number variation1nstd206human GRCh38 chr15: 43,718,874-43,744,874 , GRCh37.p13 chr15: 44,011,072-44,037,072 RNU6-354P, PDIA3, 1 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380053translocation1nstd200human GRCh38 chr15: 43,755,295-43,755,295 , GRCh38 chr15: 43,626,868-43,626,868 , GRCh37.p13 chr15: 43,919,066-43,919,066 , GRCh37.p13 chr15: 44,047,493-44,047,493 CATSPER2, PDIA3
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