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Items: 1 to 20 of 98

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7068275inversion1nstd229human GRCh38 chr9: 124,258,169-124,260,324 , GRCh37.p13 chr9: 127,020,448-127,022,603 LOC613206, NEK6
    nsv7058764inversion1nstd229human GRCh38 chr9: 124,259,061-124,260,015 , GRCh37.p13 chr9: 127,021,340-127,022,294 NEK6, LOC613206
    nsv6871369copy number variation1nstd229human GRCh38 chr9: 124,004,801-124,370,400 , GRCh37.p13 chr9: 126,767,080-127,132,679 LHX2, PSMB7, 5 more genes
    nsv6866508copy number variation1nstd229human GRCh38 chr9: 124,216,654-124,258,623 , GRCh37.p13 chr9: 126,978,933-127,020,902 LOC613206, NEK6
    nsv6866348copy number variation1nstd229human GRCh38 chr9: 124,150,196-124,269,738 , GRCh37.p13 chr9: 126,912,475-127,032,017 LOC613206, NEK6
    nsv6860023copy number variation1nstd229human GRCh38 chr9: 124,259,433-124,342,224 , GRCh37.p13 chr9: 127,021,712-127,104,503 NEK6, LOC613206
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 PBX3-DT, ADGRD2, 119 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
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313980copy number variation1nstd102humanUncertain significance GRCh37 chr9: 126,938,795-127,335,905 , GRCh38.p12 chr9: 124,176,516-124,573,626 ADGRD2, LOC100129034, 6 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6137443copy number variation1nstd213human GRCh37 chr9: 126,390,000-129,240,001 , GRCh38.p12 chr9: 123,627,721-126,477,722 NR6A1, GOLGA1, 52 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4191265copy number variation1nstd166human GRCh37.p13 chr9: 127,019,543-127,019,646 , GRCh38.p12 chr9: 124,257,264-124,257,367 LOC613206, NEK6
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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