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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094366copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,526,072-35,087,019 , GRCh38.p12 chr15: 34,233,871-34,794,818 NUTM1, ACTC1, 16 more genes
    nsv7071130inversion1nstd229human GRCh38 chr15: 33,339,608-35,270,089 , GRCh37.p13 chr15: 33,631,809-35,562,290 LOC105370765, AQR, 38 more genes
    nsv7063469inversion1nstd229human GRCh38 chr15: 33,686,568-35,388,285 , GRCh37.p13 chr15: 33,978,769-35,680,486 NUTM1, AVEN, 41 more genes
    nsv6976381copy number variation1nstd229human GRCh38 chr15: 34,365,254-34,365,532 , GRCh37.p13 chr15: 34,657,455-34,657,733 LPCAT4
    nsv6969948copy number variation1nstd229human GRCh38 chr15: 32,139,827-34,373,967 , GRCh37.p13 chr15: 32,432,028-34,666,168 AVEN, LPCAT4, 50 more genes
    nsv6634442copy number variation1nstd102humanPathogenic GRCh37 chr15: 32,915,722-34,671,601 , GRCh38.p12 chr15: 32,623,521-34,379,400 KATNBL1, ARHGAP11A, 27 more genes
    nsv6623247copy number variation1nstd224human GRCh37 chr15: 34,655,021-34,967,574 , GRCh38.p12 chr15: 34,362,820-34,675,373 FSCN1P1, LPCAT4, 10 more genes
    nsv6623246copy number variation1nstd224human GRCh37 chr15: 34,651,912-34,967,574 , GRCh38.p12 chr15: 34,359,711-34,675,373 FSCN1P1, LPCAT4, 10 more genes
    nsv6623245copy number variation1nstd224human GRCh37 chr15: 34,567,569-34,666,301 , GRCh38.p12 chr15: 34,275,368-34,374,100 LPCAT4, NOP10, 3 more genes
    nsv6505650copy number variation1nstd223human GRCh38 chr15: 34,360,601-34,452,700 , GRCh37.p13 chr15: 34,652,802-34,744,901 LOC100422491, ACTG1P15, 3 more genes
    nsv6502869copy number variation1nstd223human GRCh38 chr15: 33,970,001-34,711,900 , GRCh37.p13 chr15: 34,262,202-35,004,101 LINC02252, GOLGA8A, 20 more genes
    nsv6499953copy number variation1nstd223human GRCh38 chr15: 34,309,901-34,595,700 , GRCh37.p13 chr15: 34,602,102-34,887,901 LPCAT4, GOLGA8B, 12 more genes
    nsv6497589copy number variation1nstd223human GRCh38 chr15: 34,329,701-34,561,700 , GRCh37.p13 chr15: 34,621,902-34,853,901 SLC12A6, ACTG1P15, 12 more genes
    nsv6497505copy number variation1nstd223human GRCh38 chr15: 32,139,826-34,373,966 , GRCh37.p13 chr15: 32,432,027-34,666,167 TMCO5B, LPCAT4, 50 more genes
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6309784copy number variation1nstd102humanUncertain significance GRCh37 chr15: 34,526,082-35,087,009 , GRCh38.p12 chr15: 34,233,881-34,794,808 NUTM1, DNM1P5, 16 more genes
    nsv6132891copy number variation1nstd213human GRCh37 chr15: 34,380,000-34,660,001 , GRCh38.p12 chr15: 34,087,799-34,367,800 SLC12A6, EMC4, 6 more genes
    nsv6028830copy number variation1nstd212human GRCh38 chr15: 34,367,227-34,367,285 , GRCh37.p13 chr15: 34,659,428-34,659,486 LPCAT4
    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
    nsv5273531copy number variation1nstd204human GRCh38.p13 chr15: 33,908,501-34,437,400 , GRCh37.p13 chr15: 34,200,702-34,729,601 , GOLGA8A, 14 more genes
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