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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137874insertion1nstd232human GRCh37.p13 chr3: 15,779,029-15,779,029 , GRCh38.p12 chr3: 15,737,522-15,737,522 RN7SL4P, ANKRD28, 1 more genes
    nsv6713913copy number variation1nstd229human GRCh38 chr3: 15,740,863-15,746,789 , GRCh37.p13 chr3: 15,782,370-15,788,296 LOC101927647, 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
    nsv6712653copy number variation1nstd229human GRCh38 chr3: 15,761,601-15,768,900 , GRCh37.p13 chr3: 15,803,108-15,810,407 ANKRD28, LOC101927647
    nsv6706513copy number variation1nstd229human GRCh38 chr3: 15,761,243-15,764,273 , GRCh37.p13 chr3: 15,802,750-15,805,780 ANKRD28, LOC101927647
    nsv6705962copy number variation1nstd229human GRCh38 chr3: 15,737,326-15,741,257 , GRCh37.p13 chr3: 15,778,833-15,782,764 LOC101927647, RN7SL4P, 1 more genes
    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
    nsv6374236copy number variation1nstd223human GRCh38 chr3: 15,734,101-15,755,500 , GRCh37.p13 chr3: 15,775,608-15,797,007 LOC101927647, ANKRD28, 1 more genes
    nsv6372529copy number variation1nstd223human GRCh38 chr3: 15,756,519-15,758,466 , GRCh37.p13 chr3: 15,798,026-15,799,973 LOC101927647, ANKRD28
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv6291013copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,085,863-16,402,392 , GRCh38.p12 chr3: 15,044,356-16,360,885 MIR563, RNU6-1024P, 30 more genes
    nsv6253733mobile element insertion1nstd215human GRCh38 chr3: 15,741,737-15,741,737 , GRCh37.p13 chr3: 15,783,244-15,783,244 LOC101927647, ANKRD28
    nsv6042522insertion1nstd212human GRCh38 chr3: 15,737,522-15,737,522 , GRCh37.p13 chr3: 15,779,029-15,779,029 RN7SL4P, ANKRD28, 1 more genes
    nsv6040626insertion1nstd212human GRCh38 chr3: 15,742,696-15,742,696 , GRCh37.p13 chr3: 15,784,203-15,784,203 ANKRD28, LOC101927647
    nsv5949462insertion1nstd209human GRCh37.p13 chr3: 15,779,029-15,779,029 , GRCh38 chr3: 15,737,522-15,737,522 RN7SL4P, ANKRD28, 1 more genes
    nsv5694049mobile element insertion1nstd211human GRCh38 chr3: 15,741,737-15,741,737 , GRCh37.p13 chr3: 15,783,244-15,783,244 LOC101927647, ANKRD28
    nsv5608029insertion1nstd207human GRCh38 chr3: 15,742,688-15,742,688 , GRCh37.p13 chr3: 15,784,195-15,784,195 ANKRD28, LOC101927647
    nsv5606614insertion1nstd207human GRCh38 chr3: 15,737,522-15,737,522 , GRCh37.p13 chr3: 15,779,029-15,779,029 RN7SL4P, ANKRD28, 1 more genes
    nsv5207447copy number variation1nstd204human GRCh38.p13 chr3: 15,750,564-15,752,595 , GRCh37.p13 chr3: 15,792,071-15,794,102 LOC101927647, ANKRD28
    nsv5196361mobile element insertion1nstd203human GRCh38 chr3: 15,741,696-15,741,737 , GRCh37.p13 chr3: 15,783,203-15,783,244 ANKRD28, LOC101927647
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