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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv7097097copy number variation1nstd102humanUncertain significance GRCh37 chr6: 84,765,038-86,267,798 , GRCh38.p12 chr6: 84,055,319-85,558,080 MRAP2, LOC107986619, 18 more genes
    nsv7055908inversion1nstd229human GRCh38 chr6: 84,727,364-84,727,402 , GRCh37.p13 chr6: 85,437,082-85,437,120 TBX18
    nsv7046331inversion1nstd229human GRCh38 chr6: 84,428,655-84,685,605 , GRCh37.p13 chr6: 85,138,373-85,395,323 TBX18, LINC01611, 2 more genes
    nsv7045407inversion1nstd229human GRCh38 chr6: 84,691,916-84,697,139 , GRCh37.p13 chr6: 85,401,634-85,406,857 TBX18-AS1, TBX18
    nsv6817090copy number variation1nstd229human GRCh38 chr6: 84,677,076-84,683,862 , GRCh37.p13 chr6: 85,386,794-85,393,580 TBX18
    nsv6816898copy number variation1nstd229human GRCh38 chr6: 84,677,001-84,678,800 , GRCh37.p13 chr6: 85,386,719-85,388,518 TBX18
    nsv6816120copy number variation1nstd229human GRCh38 chr6: 84,757,601-84,760,200 , GRCh37.p13 chr6: 85,467,319-85,469,918 TBX18
    nsv6814901copy number variation1nstd229human GRCh38 chr6: 84,735,726-84,735,790 , GRCh37.p13 chr6: 85,445,444-85,445,508 TBX18
    nsv6813812copy number variation1nstd229human GRCh38 chr6: 84,677,072-84,683,862 , GRCh37.p13 chr6: 85,386,790-85,393,580 TBX18
    nsv6811561copy number variation1nstd229human GRCh38 chr6: 84,722,050-85,204,443 , GRCh37.p13 chr6: 85,431,768-85,914,161 TBX18, LOC100421583, 1 more genes
    nsv6810944copy number variation1nstd229human GRCh38 chr6: 84,691,244-84,725,457 , GRCh37.p13 chr6: 85,400,962-85,435,175 TBX18, TBX18-AS1
    nsv6807380copy number variation1nstd229human GRCh38 chr6: 84,687,775-84,687,869 , GRCh37.p13 chr6: 85,397,493-85,397,587 TBX18, TBX18-AS1
    nsv6804093copy number variation1nstd229human GRCh38 chr6: 84,673,221-84,680,148 , GRCh37.p13 chr6: 85,382,939-85,389,866 TBX18
    nsv6803630copy number variation1nstd229human GRCh38 chr6: 84,680,048-84,750,393 , GRCh37.p13 chr6: 85,389,766-85,460,111 TBX18-AS1, TBX18
    nsv6798707copy number variation1nstd229human GRCh38 chr6: 84,679,042-84,683,772 , GRCh37.p13 chr6: 85,388,760-85,393,490 TBX18
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631335copy number variation1nstd224human GRCh37 chr6: 85,473,722-85,521,035 , GRCh38.p12 chr6: 84,764,004-84,811,317 TBX18
    nsv6562641inversion1nstd223human GRCh38 chr6: 84,595,873-85,427,122 , GRCh37.p13 chr6: 85,305,591-86,136,840 LOC100421093, LOC100421583, 9 more genes
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