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Items: 1 to 20 of 309

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905069copy number variation1nstd209human GRCh38 chr3: 15,703,967-15,706,239 , GRCh37.p13 chr3: 15,745,474-15,747,746 BTD, ANKRD28
    nsv5901097copy number variation1nstd209human GRCh38 chr3: 15,622,497-15,622,635 , GRCh37.p13 chr3: 15,664,004-15,664,142 BTD
    nsv5900919copy number variation1nstd209human GRCh38 chr3: 15,654,684-15,654,846 , GRCh37.p13 chr3: 15,696,191-15,696,353 BTD
    nsv5834381copy number variation1nstd209human GRCh38 chr3: 15,703,983-15,706,257 , GRCh37.p13 chr3: 15,745,490-15,747,764 ANKRD28, BTD
    nsv5691318mobile element insertion2nstd211human GRCh38 chr3: 15,655,320-15,655,320 , GRCh37.p13 chr3: 15,696,827-15,696,827 BTD
    nsv5687719mobile element insertion2nstd211human GRCh38 chr3: 15,613,191-15,613,191 , GRCh37.p13 chr3: 15,654,698-15,654,698 BTD
    nsv5673638copy number variation1nstd102humanPathogenic GRCh37 chr3: 15,683,405-15,687,154 , GRCh38.p12 chr3: 15,641,898-15,645,647 BTD
    nsv5449098copy number variation1nstd206human GRCh38 chr3: 15,643,948-15,644,079 , GRCh37.p13 chr3: 15,685,455-15,685,586 BTD
    nsv5412380mobile element insertion1nstd206human GRCh38 chr3: 15,655,320-15,655,371 , GRCh37.p13 chr3: 15,696,827-15,696,878 BTD
    nsv5401674mobile element insertion1nstd206human GRCh38 chr3: 15,613,191-15,613,242 , GRCh37.p13 chr3: 15,654,698-15,654,749 BTD
    nsv5377358translocation1nstd200human GRCh38 chr2: 222,546,759-222,546,759 , GRCh38 chr3: 15,668,928-15,668,928 , GRCh37.p13 chr2: 223,411,478-223,411,478 , GRCh37.p13 chr3: 15,710,435-15,710,435 BTD, ANKRD28, 1 more genes
    nsv5367007translocation1nstd200human GRCh38 chr3: 15,699,623-15,699,623 , GRCh38 chr3: 15,706,911-15,706,911 , GRCh37.p13 chr3: 15,748,418-15,748,418 , GRCh37.p13 chr3: 15,741,130-15,741,130 ANKRD28, BTD
    nsv5366836translocation1nstd200human GRCh38 chr2: 222,546,767-222,546,767 , GRCh38 chr3: 15,668,596-15,668,596 , GRCh37.p13 chr2: 223,411,486-223,411,486 , GRCh37.p13 chr3: 15,710,103-15,710,103 BTD, ANKRD28, 1 more genes
    nsv5351474translocation1nstd200human GRCh38 chr3: 15,676,744-15,676,744 , GRCh38 chr3: 15,676,856-15,676,856 , GRCh37.p13 chr3: 15,718,251-15,718,251 , GRCh37.p13 chr3: 15,718,363-15,718,363 BTD, ANKRD28
    nsv5312037copy number variation1nstd204human GRCh38.p13 chr3: 15,654,869-15,655,847 , GRCh37.p13 chr3: 15,696,376-15,697,354 BTD
    nsv5185374mobile element insertion1nstd203human GRCh38 chr3: 15,663,554-15,663,569 , GRCh37.p13 chr3: 15,705,061-15,705,076 BTD
    nsv5079609mobile element insertion1nstd203human GRCh38 chr3: 15,646,870-15,646,886 , GRCh37.p13 chr3: 15,688,377-15,688,393 BTD
    nsv5079367mobile element insertion1nstd203human GRCh38 chr3: 15,617,214-15,617,231 , GRCh37.p13 chr3: 15,658,721-15,658,738 BTD
    nsv5079213mobile element insertion1nstd203human GRCh38 chr3: 15,718,606-15,718,619 , GRCh37.p13 chr3: 15,760,113-15,760,126 ANKRD28, BTD
    nsv5070719mobile element insertion1nstd203human GRCh38 chr3: 15,634,204-15,634,218 , GRCh37.p13 chr3: 15,675,711-15,675,725 BTD
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