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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7065334inversion1nstd229human GRCh38 chr15: 93,747,426-97,526,629 , GRCh37.p13 chr15: 94,290,655-98,069,859 NR2F2-AS1, LOC440311, 46 more genes
    nsv6968676copy number variation1nstd229human GRCh38 chr15: 96,334,603-96,337,344 , GRCh37.p13 chr15: 96,877,832-96,880,573 NR2F2
    nsv6962395copy number variation1nstd229human GRCh38 chr15: 96,304,042-96,363,315 , GRCh37.p13 chr15: 96,847,271-96,906,544 MIR1469, NR2F2, 2 more genes
    nsv6960547copy number variation1nstd229human GRCh38 chr15: 93,794,809-100,070,222 , GRCh37.p13 chr15: 94,338,038-100,610,427 LOC105371010, LOC105371007, 81 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6513896copy number variation1nstd223human GRCh38 chr15: 96,329,501-96,335,300 , GRCh37.p13 chr15: 96,872,730-96,878,529 MIR1469, NR2F2
    nsv6510544copy number variation1nstd223human GRCh38 chr15: 96,330,501-96,335,500 , GRCh37.p13 chr15: 96,873,730-96,878,729 MIR1469, NR2F2
    nsv6313944copy number variation1nstd102humanPathogenic GRCh37 chr15: 94,836,128-101,302,111 , GRCh38.p12 chr15: 94,292,899-100,761,906 LINC01582, LRRC28, 85 more genes
    nsv6309982copy number variation1nstd102humanUncertain significance GRCh37 chr15: 96,875,335-96,880,851 , GRCh38.p12 chr15: 96,332,106-96,337,622 NR2F2, MIR1469
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132970copy number variation1nstd213human GRCh37 chr15: 94,940,000-102,531,392 , GRCh38.p12 chr15: 94,396,771-101,981,189 ALDH1A3, PCSK6, 124 more genes
    nsv6132919copy number variation1nstd213human GRCh37 chr15: 91,580,000-100,660,001 , GRCh38.p12 chr15: 91,036,770-100,119,796 ST8SIA2, SYNM, 116 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5938972copy number variation1nstd209human GRCh38 chr15: 95,301,994-96,435,598 , GRCh37.p13 chr15: 95,845,223-96,978,828 , RNU2-3P, 13 more genes
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4619556copy number variation1nstd183human GRCh37 chr15: 96,873,503-96,874,703 , GRCh38.p12 chr15: 96,330,274-96,331,474 MIR1469, NR2F2
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