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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096700copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,643,358-15,687,154 , GRCh38.p12 chr3: 15,601,851-15,645,647 BTD, HACL1
    nsv7096544copy number variation1nstd102humanPathogenic GRCh37 chr3: 15,512,023-15,687,154 , GRCh38.p12 chr3: 15,470,516-15,645,647 BTD, RN7SL110P, 3 more genes
    nsv6715274copy number variation1nstd229human GRCh38 chr3: 15,680,765-15,680,784 , GRCh37.p13 chr3: 15,722,272-15,722,291 BTD, ANKRD28
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6712405copy number variation1nstd229human GRCh38 chr3: 15,641,841-15,654,836 , GRCh37.p13 chr3: 15,683,348-15,696,343 BTD
    nsv6711010copy number variation1nstd229human GRCh38 chr3: 15,602,890-15,607,546 , GRCh37.p13 chr3: 15,644,397-15,649,053 BTD
    nsv6707492copy number variation1nstd229human GRCh38 chr3: 15,605,763-15,661,016 , GRCh37.p13 chr3: 15,647,270-15,702,523 BTD
    nsv6704843copy number variation1nstd229human GRCh38 chr3: 15,653,155-15,660,515 , GRCh37.p13 chr3: 15,694,662-15,702,022 BTD
    nsv6701140copy number variation1nstd229human GRCh38 chr3: 15,688,121-15,688,147 , GRCh37.p13 chr3: 15,729,628-15,729,654 BTD, ANKRD28
    nsv6700128copy number variation1nstd229human GRCh38 chr3: 15,605,953-15,614,327 , GRCh37.p13 chr3: 15,647,460-15,655,834 BTD
    nsv6699051copy number variation1nstd229human GRCh38 chr3: 15,610,389-15,611,104 , GRCh37.p13 chr3: 15,651,896-15,652,611 BTD
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6548914inversion1nstd223human GRCh38 chr3: 15,639,802-15,640,399 , GRCh37.p13 chr3: 15,681,309-15,681,906 BTD
    nsv6545884inversion1nstd223human GRCh38 chr3: 15,616,444-15,617,025 , GRCh37.p13 chr3: 15,657,951-15,658,532 BTD
    nsv6543842inversion1nstd223human GRCh38 chr3: 15,661,004-15,663,149 , GRCh37.p13 chr3: 15,702,511-15,704,656 BTD
    nsv6542455inversion1nstd223human GRCh38 chr3: 15,690,634-15,692,084 , GRCh37.p13 chr3: 15,732,141-15,733,591 BTD, ANKRD28
    nsv6373203copy number variation1nstd223human GRCh38 chr3: 15,667,659-15,668,179 , GRCh37.p13 chr3: 15,709,166-15,709,686 ANKRD28, BTD
    nsv6358111copy number variation1nstd223human GRCh38 chr3: 15,610,361-15,611,028 , GRCh37.p13 chr3: 15,651,868-15,652,535 BTD
    nsv6358076copy number variation1nstd223human GRCh38 chr3: 15,670,834-15,671,864 , GRCh37.p13 chr3: 15,712,341-15,713,371 ANKRD28, BTD
    nsv6355620copy number variation1nstd223human GRCh38 chr3: 15,654,803-15,655,871 , GRCh37.p13 chr3: 15,696,310-15,697,378 BTD
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