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Items: 1 to 20 of 210

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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
    nsv7052981inversion1nstd229human GRCh38 chr6: 167,557,448-168,005,975 , GRCh37.p13 chr6: 168,042,074-168,406,655 LINC01558, LOC105378130, 12 more genes
    nsv7051730inversion1nstd229human GRCh38 chr6: 167,665,486-170,032,054 , GRCh37.p13 chr6: 168,066,166-170,347,278 WDR27, KIF25, 49 more genes
    nsv7050840inversion1nstd229human GRCh38 chr6: 167,446,684-167,820,665 , GRCh37.p13 chr6: 167,858,901-168,221,345 LOC105378131, LOC105378128, 10 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
    nsv7039039inversion1nstd229human GRCh38 chr6: 167,430,213-167,810,516 , GRCh37.p13 chr6: 167,843,701-168,211,196 LOC105378127, LOC105378130, 11 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
    nsv6815355copy number variation1nstd229human GRCh38 chr6: 167,731,601-167,757,200 , GRCh37.p13 chr6: 168,132,281-168,157,880 LOC107986547
    nsv6811640copy number variation1nstd229human GRCh38 chr6: 167,513,619-167,811,020 , GRCh37.p13 chr6: 167,925,811-168,211,700 LINC02538, LOC105378131, 7 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
    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
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6631120copy number variation1nstd224human GRCh37 chr6: 167,687,856-168,203,445 , GRCh38.p12 chr6: 167,274,368-167,802,765 LOC441179, LOC105378128, 15 more genes
    nsv6631119copy number variation1nstd224human GRCh37 chr6: 167,685,688-168,203,445 , GRCh38.p12 chr6: 167,272,200-167,802,765 LOC441179, LOC105378128, 15 more genes
    nsv6630934copy number variation1nstd224human GRCh37 chr6: 167,789,455-168,204,222 , GRCh38.p12 chr6: 167,375,967-167,803,542 LOC105378128, LOC107986546, 12 more genes
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6315394copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,770,398-170,919,482 , GRCh38.p12 chr6: 167,356,910-170,610,394 LINC02544, LOC107986676, 72 more genes
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