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Items: 1 to 20 of 178

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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
    nsv7055465inversion1nstd229human GRCh38 chr6: 166,312,530-166,346,578 , GRCh37.p13 chr6: 166,726,018-166,760,066 SFT2D1, HNRNPA1P49, 2 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
    nsv6816043copy number variation1nstd229human GRCh38 chr6: 165,919,144-166,571,192 , GRCh37.p13 chr6: 166,332,632-166,984,680 HNRNPA1P49, MIR1913, 19 more genes
    nsv6812358copy number variation1nstd229human GRCh38 chr6: 166,349,180-166,349,353 , GRCh37.p13 chr6: 166,762,668-166,762,841 LOC100289495
    nsv6807032copy number variation1nstd229human GRCh38 chr6: 166,264,628-166,373,652 , GRCh37.p13 chr6: 166,678,116-166,787,140 LOC105378118, SFT2D1, 5 more genes
    nsv6799827copy number variation1nstd229human GRCh38 chr6: 166,333,127-166,341,672 , GRCh37.p13 chr6: 166,746,615-166,755,160 SFT2D1, HNRNPA1P49, 1 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
    nsv6556844inversion1nstd223human GRCh38 chr6: 161,649,493-166,382,472 , GRCh37.p13 chr6: 162,070,525-166,795,960 RNU6-730P, TRE-TTC15-1, 49 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
    nsv6313793copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,212,864-170,919,482 , GRCh38.p12 chr6: 161,791,832-170,610,394 LOC645468, GPR31, 148 more genes
    nsv6313745copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,290,087-170,919,482 , GRCh38.p12 chr6: 162,869,055-170,610,394 HGC6.3, LOC112267970, 143 more genes
    nsv6313560copy number variation1nstd102humanPathogenic GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394 LOC105378142, LOC100289495, 159 more genes
    nsv4968655copy number variation1nstd200human GRCh38 chr6: 165,587,706-166,398,601 , GRCh37.p13 chr6: 166,001,194-166,812,089 LOC105378115, TBXT, 19 more genes
    nsv4965927copy number variation1nstd200human GRCh38 chr6: 166,346,519-166,346,600 , GRCh37.p13 chr6: 166,760,007-166,760,088 LOC100289495
    nsv4824887copy number variation1nstd200human GRCh37 chr6: 166,001,194-166,812,089 , GRCh38.p12 chr6: 165,587,706-166,398,601 GNG5P1, LOC107986668, 19 more genes
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
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