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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072115inversion1nstd229human GRCh38 chr9: 12,276,809-15,153,662 , GRCh37.p13 chr9: 12,276,809-15,153,660 PES1P2, RNU6-559P, 30 more genes
    nsv7068293inversion1nstd229human GRCh38 chr9: 12,453,912-21,375,878 , GRCh37.p13 chr9: 12,453,912-21,375,877 RNU6-264P, PSMC3P1, 115 more genes
    nsv7062404inversion1nstd229human GRCh38 chr9: 12,646,715-21,082,028 , GRCh37.p13 chr9: 12,646,715-21,082,027 RPS6, RPL7AP47, 95 more genes
    nsv6876108copy number variation1nstd229human GRCh38 chr9: 13,348,301-13,573,300 , GRCh37.p13 chr9: 13,348,300-13,573,299 LOC105375977, LINC01235
    nsv6875984copy number variation1nstd229human GRCh38 chr9: 12,949,792-14,402,752 , GRCh37.p13 chr9: 12,949,791-14,402,751 LINC00583, LOC101929507, 11 more genes
    nsv6875320copy number variation1nstd229human GRCh38 chr9: 13,390,274-13,413,951 , GRCh37.p13 chr9: 13,390,273-13,413,950 LINC01235
    nsv6869767copy number variation1nstd229human GRCh38 chr9: 10,284,542-14,203,331 , GRCh37.p13 chr9: 10,284,542-14,203,330 LINC01235, TYRP1, 26 more genes
    nsv6865625copy number variation1nstd229human GRCh38 chr9: 12,877,282-13,877,411 , GRCh37.p13 chr9: 12,877,281-13,877,410 PRDX1P1, LOC101929507, 5 more genes
    nsv6863376copy number variation1nstd229human GRCh38 chr9: 13,259,101-13,535,900 , GRCh37.p13 chr9: 13,259,100-13,535,899 LINC01235, LOC105375977, 1 more genes
    nsv6861987copy number variation1nstd229human GRCh38 chr9: 12,898,301-13,877,400 , GRCh37.p13 chr9: 12,898,300-13,877,399 LOC100130801, LINC01235, 5 more genes
    nsv6861052copy number variation1nstd229human GRCh38 chr9: 13,345,501-13,573,000 , GRCh37.p13 chr9: 13,345,500-13,572,999 LOC105375977, LINC01235
    nsv6860421copy number variation1nstd229human GRCh38 chr9: 5,097,512-15,003,390 , GRCh37.p13 chr9: 5,097,512-15,003,388 LOC102724027, ATP5PDP3, 89 more genes
    nsv6858879copy number variation1nstd229human GRCh38 chr9: 13,422,595-13,422,871 , GRCh37.p13 chr9: 13,422,594-13,422,870 LINC01235
    nsv6858774copy number variation1nstd229human GRCh38 chr9: 13,428,765-13,433,687 , GRCh37.p13 chr9: 13,428,764-13,433,686 LINC01235
    nsv6858691copy number variation1nstd229human GRCh38 chr9: 12,722,371-13,540,765 , GRCh37.p13 chr9: 12,722,370-13,540,764 LOC100130801, RN7SL849P, 7 more genes
    nsv6637883copy number variation1nstd102humanPathogenic GRCh37 chr9: 13,122,130-13,649,715 , GRCh38.p12 chr9: 13,122,131-13,649,716 MPDZ, LINC01235, 1 more genes
    nsv6637566copy number variation1nstd102humanUncertain significance GRCh37 chr9: 12,356,017-13,444,934 , GRCh38.p12 chr9: 12,356,017-13,444,935 TYRP1, RN7SL849P, 8 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634450copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,048,247 , GRCh38.p12 chr9: 203,861-15,048,249 LOC102724027, DMRT2, 157 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
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