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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5855151copy number variation2nstd209human GRCh38 chr12: 51,333,283-51,334,482 , GRCh37.p13 chr12: 51,727,067-51,728,266 CELA1
    nsv5704672mobile element insertion2nstd211human GRCh38 chr12: 51,326,609-51,326,609 , GRCh37.p13 chr12: 51,720,393-51,720,393 CELA1
    nsv5506503copy number variation1nstd206human GRCh38 chr12: 51,329,545-51,329,597 , GRCh37.p13 chr12: 51,723,329-51,723,381 CELA1
    nsv5427439mobile element insertion1nstd206human GRCh38 chr12: 51,326,609-51,326,660 , GRCh37.p13 chr12: 51,720,393-51,720,444 CELA1
    nsv5139924mobile element insertion1nstd203human GRCh38 chr12: 51,340,776-51,340,786 , GRCh37.p13 chr12: 51,734,560-51,734,570 CELA1
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4985593copy number variation1nstd200human GRCh38 chr12: 51,321,451-51,333,333 , GRCh37.p13 chr12: 51,715,235-51,727,117 CELA1, LOC105369767, 1 more genes
    nsv4985592copy number variation1nstd200human GRCh38 chr12: 51,295,210-51,331,314 , GRCh37.p13 chr12: 51,688,994-51,725,098 BIN2, LOC105369767, 1 more genes
    nsv4972674copy number variation1nstd200human GRCh38 chr12: 51,333,038-51,334,600 , GRCh37.p13 chr12: 51,726,822-51,728,384 CELA1
    nsv4972673copy number variation1nstd200human GRCh38 chr12: 51,326,369-51,328,198 , GRCh37.p13 chr12: 51,720,153-51,721,982 CELA1
    nsv4842053copy number variation1nstd200human GRCh37 chr12: 51,688,994-51,725,098 , GRCh38.p12 chr12: 51,295,210-51,331,314 CELA1, LOC105369767, 1 more genes
    nsv4834759copy number variation1nstd200human GRCh37 chr12: 51,720,153-51,721,982 , GRCh38.p12 chr12: 51,326,369-51,328,198 CELA1
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4681022copy number variation1nstd189human GRCh37.p13 chr12: 51,686,728-51,877,403 , GRCh38.p12 chr12: 51,292,944-51,483,619 , CELA1, 5 more genes
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4204098copy number variation1nstd166human GRCh37.p13 chr12: 51,723,329-51,723,381 , GRCh38.p12 chr12: 51,329,545-51,329,597 CELA1
    nsv4197410copy number variation1nstd166human GRCh37.p13 chr12: 51,723,000-51,728,000 , GRCh38.p12 chr12: 51,329,216-51,334,216 CELA1
    nsv3924549copy number variation1nstd102humanPathogenic GRCh37 chr12: 51,027,671-53,245,693 , GRCh38 chr12: 50,633,888-52,851,909 , NCBI36 chr12: 49,313,938-51,531,960 KRT128P, KRT80, 82 more genes
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