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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074157inversion1nstd229human GRCh38 chr14: 51,800,664-53,760,846 , GRCh37.p13 chr14: 52,267,382-54,227,564 GNPNAT1, LOC102723604, 26 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7060630inversion1nstd229human GRCh38 chr14: 52,064,707-52,703,250 , GRCh37.p13 chr14: 52,531,425-53,169,968 LOC105378180, GPR137C, 8 more genes
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6952335copy number variation1nstd229human GRCh38 chr14: 52,324,159-52,324,240 , GRCh37.p13 chr14: 52,790,877-52,790,958 PTGER2
    nsv6949862copy number variation1nstd229human GRCh38 chr14: 51,123,112-56,995,885 , GRCh37.p13 chr14: 51,589,830-57,462,603 RPL3P3, RNA5SP385, 96 more genes
    nsv6938412copy number variation1nstd229human GRCh38 chr14: 46,367,427-52,468,480 , GRCh37.p13 chr14: 46,836,630-52,935,198 RNU6-297P, RN7SL452P, 95 more genes
    nsv6578746inversion1nstd223human GRCh38 chr14: 49,838,941-56,572,992 , GRCh37.p13 chr14: 50,305,659-57,039,710 LOC100419913, TXNDC16, 124 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6133131copy number variation1nstd213human GRCh37 chr14: 52,470,000-55,150,001 , GRCh38.p12 chr14: 52,003,282-54,683,283 PSMC6, PTGER2, 35 more genes
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5701257mobile element insertion2nstd211human GRCh38 chr14: 52,313,728-52,313,728 , GRCh37.p13 chr14: 52,780,446-52,780,446 PTGER2
    nsv5663484insertion1nstd207human GRCh38 chr14: 52,313,728-52,313,728 , GRCh37.p13 chr14: 52,780,446-52,780,446 PTGER2
    nsv5559453sequence alteration1nstd206human GRCh38 chr14: 52,308,604-52,339,517 , GRCh37.p13 chr14: 52,775,322-52,806,235 PTGER2
    nsv5546789insertion1nstd206human GRCh38 chr14: 52,313,728-52,313,779 , GRCh37.p13 chr14: 52,780,446-52,780,497 PTGER2
    nsv5184433mobile element insertion1nstd203human GRCh38 chr14: 52,323,832-52,323,848 , GRCh37.p13 chr14: 52,790,550-52,790,566 PTGER2
    nsv5146344mobile element insertion1nstd203human GRCh38 chr14: 52,313,728-52,313,728 , GRCh37.p13 chr14: 52,780,446-52,780,446 PTGER2
    nsv4728859copy number variation1nstd102humanUncertain significance GRCh37 chr14: 52,566,666-52,846,237 , GRCh38.p12 chr14: 52,099,948-52,379,519 PTGDR, COX5AP2, 3 more genes
    nsv4675343copy number variation1nstd102humanUncertain significance GRCh37 chr14: 52,727,933-52,809,716 , GRCh38.p12 chr14: 52,261,215-52,342,998 PTGDR, PTGER2, 1 more genes
    nsv4540825insertion1nstd166human GRCh37.p13 chr14: 52,780,446-52,780,446 , GRCh38.p12 chr14: 52,313,728-52,313,728 PTGER2
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