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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7058070inversion1nstd229human GRCh38 chr6: 167,360,912-167,407,360 , GRCh37.p13 chr6: 167,774,400-167,820,848 TCP10L3
    nsv7055822inversion1nstd229human GRCh38 chr6: 167,162,129-167,419,068 , GRCh37.p13 chr6: 167,575,617-167,832,556 LOC102725048, LOC100421518, 8 more genes
    nsv7053853inversion1nstd229human GRCh38 chr6: 167,308,591-167,487,580 , GRCh37.p13 chr6: 167,722,079-167,899,772 UNC93A, TCP10L3, 5 more genes
    nsv7049628inversion1nstd229human GRCh38 chr6: 167,174,588-167,397,247 , GRCh37.p13 chr6: 167,588,076-167,810,735 TCP10L2, LOC100421518, 7 more genes
    nsv7047951inversion1nstd229human GRCh38 chr6: 167,351,568-167,810,519 , GRCh37.p13 chr6: 167,765,056-168,211,199 TCP10L3, LOC100422263, 12 more genes
    nsv7046230inversion1nstd229human GRCh38 chr6: 167,229,870-167,473,034 , GRCh37.p13 chr6: 167,643,358-167,885,257 TTLL2, LOC102725048, 7 more genes
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv7038888inversion1nstd229human GRCh38 chr6: 167,222,887-168,363,767 , GRCh37.p13 chr6: 167,636,375-168,764,447 LOC101929420, LOC102724220, 32 more genes
    nsv6817934copy number variation1nstd229human GRCh38 chr6: 167,045,707-167,831,746 , GRCh37.p13 chr6: 167,459,195-168,232,426 LOC105378123, LOC105378126, 28 more genes
    nsv6814800copy number variation1nstd229human GRCh38 chr6: 167,235,001-167,417,200 , GRCh37.p13 chr6: 167,648,489-167,830,688 LOC102724220, HPAT5, 5 more genes
    nsv6812622copy number variation1nstd229human GRCh38 chr6: 167,162,890-167,427,832 , GRCh37.p13 chr6: 167,576,378-167,841,320 TCP10L2, HPAT5, 9 more genes
    nsv6811648copy number variation1nstd229human GRCh38 chr6: 167,294,642-167,542,413 , GRCh37.p13 chr6: 167,708,130-167,942,073 TCP10L3, TTLL2, 6 more genes
    nsv6808556copy number variation1nstd229human GRCh38 chr6: 167,250,721-167,500,657 , GRCh37.p13 chr6: 167,664,209-167,912,849 LOC105378126, TCP10L3, 5 more genes
    nsv6804037copy number variation1nstd229human GRCh38 chr6: 167,372,241-167,821,337 , GRCh37.p13 chr6: 167,785,729-168,222,017 LOC107986546, LINC02538, 12 more genes
    nsv6802385copy number variation1nstd229human GRCh38 chr6: 167,155,513-167,512,188 , GRCh37.p13 chr6: 167,569,001-167,924,380 LOC107986546, LOC105378128, 13 more genes
    nsv6800765copy number variation1nstd229human GRCh38 chr6: 167,248,432-167,407,071 , GRCh37.p13 chr6: 167,661,920-167,820,559 UNC93A, LOC100421518, 2 more genes
    nsv6799972copy number variation1nstd229human GRCh38 chr6: 167,251,095-167,408,628 , GRCh37.p13 chr6: 167,664,583-167,822,116 LOC100421518, UNC93A, 2 more genes
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
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