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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094534copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,016,689-43,020,485 , GRCh38.p12 chr15: 42,724,491-42,728,287 CDAN1
    nsv7094373copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,016,689-43,398,220 , GRCh38.p12 chr15: 42,724,491-43,106,022 FDPSP4, CDAN1, 3 more genes
    nsv7065472inversion1nstd229human GRCh38 chr15: 42,733,848-42,733,900 , GRCh37.p13 chr15: 43,026,046-43,026,098 CDAN1
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6972255copy number variation1nstd229human GRCh38 chr15: 42,703,810-42,723,878 , GRCh37.p13 chr15: 42,996,008-43,016,076 STARD9, CDAN1
    nsv6970616copy number variation1nstd229human GRCh38 chr15: 42,727,588-42,727,786 , GRCh37.p13 chr15: 43,019,786-43,019,984 CDAN1
    nsv6969870copy number variation1nstd229human GRCh38 chr15: 42,709,664-42,794,279 , GRCh37.p13 chr15: 43,001,862-43,086,477 CDAN1, TTBK2, 1 more genes
    nsv6969647copy number variation1nstd229human GRCh38 chr15: 42,722,014-42,733,543 , GRCh37.p13 chr15: 43,014,212-43,025,741 CDAN1
    nsv6968366copy number variation1nstd229human GRCh38 chr15: 42,723,356-42,727,839 , GRCh37.p13 chr15: 43,015,554-43,020,037 CDAN1
    nsv6966799copy number variation1nstd229human GRCh38 chr15: 42,719,549-42,722,142 , GRCh37.p13 chr15: 43,011,747-43,014,340 STARD9, CDAN1
    nsv6132952copy number variation1nstd213human GRCh37 chr15: 42,480,000-43,110,001 , GRCh38.p12 chr15: 42,187,802-42,817,803 GANC, VPS39, 17 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5005321copy number variation1nstd200human GRCh38 chr15: 42,709,664-42,794,279 , GRCh37.p13 chr15: 43,001,862-43,086,477 CDAN1, TTBK2, 1 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4674906copy number variation1nstd102humanUncertain significance GRCh37 chr15: 43,017,718-43,685,171 , GRCh38.p12 chr15: 42,725,520-43,392,973 UBR1, CDAN1, 17 more genes
    nsv4624181copy number variation1nstd183human GRCh37 chr15: 42,852,311-43,035,603 , GRCh38.p12 chr15: 42,560,113-42,743,405 HAUS2, STARD9, 4 more genes
    nsv4559484mobile element insertion1nstd166human GRCh37.p13 chr15: 43,016,252-43,016,252 , GRCh38.p12 chr15: 42,724,054-42,724,054 CDAN1
    nsv4233841copy number variation1nstd166human GRCh37.p13 chr15: 43,014,212-43,025,738 , GRCh38.p12 chr15: 42,722,014-42,733,540 CDAN1
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