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Items: 1 to 20 of 199

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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
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv6817222copy number variation1nstd229human GRCh38 chr6: 166,378,756-166,380,458 , GRCh37.p13 chr6: 166,792,244-166,793,946 MPC1
    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
    nsv6814782copy number variation1nstd229human GRCh38 chr6: 166,372,399-166,372,459 , GRCh37.p13 chr6: 166,785,887-166,785,947 MPC1
    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
    nsv6803279copy number variation1nstd229human GRCh38 chr6: 166,375,391-166,385,604 , GRCh37.p13 chr6: 166,788,879-166,799,092 MPC1
    nsv6798929copy number variation1nstd229human GRCh38 chr6: 166,365,511-166,366,007 , GRCh37.p13 chr6: 166,778,999-166,779,495 MPC1
    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
    nsv6616581copy number variation1nstd223human GRCh38 chr6: 166,368,494-166,369,342 , GRCh37.p13 chr6: 166,781,982-166,782,830 MPC1
    nsv6601938copy number variation1nstd223human GRCh38 chr6: 166,375,391-166,385,602 , GRCh37.p13 chr6: 166,788,879-166,799,090 MPC1
    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
    nsv6180726copy number variation1nstd214human GRCh38 chr6: 166,372,399-166,372,458 , GRCh37.p13 chr6: 166,785,887-166,785,946 MPC1
    nsv6003095copy number variation1nstd212human GRCh38 chr6: 166,382,453-166,382,509 , GRCh37.p13 chr6: 166,795,941-166,795,997 MPC1
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