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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097851copy number variation1nstd102humanUncertain significance GRCh37 chr6: 82,459,412-82,461,858 , GRCh38.p12 chr6: 81,749,695-81,752,141 TENT5A
    nsv7046126inversion1nstd229human GRCh38 chr6: 81,393,479-82,767,602 , GRCh37.p13 chr6: 82,103,196-83,477,319 LOC107986617, IBTK, 12 more genes
    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
    nsv6783925copy number variation1nstd229human GRCh38 chr6: 81,691,926-82,286,650 , GRCh37.p13 chr6: 82,401,643-82,996,367 RNU6-130P, LOC105377874, 7 more genes
    nsv6779356copy number variation1nstd229human GRCh38 chr6: 80,800,138-81,949,180 , GRCh37.p13 chr6: 81,509,855-82,658,897 LOC105377873, LINC02542, 4 more genes
    nsv6636874copy number variation1nstd102humanUncertain significance GRCh37 chr6: 81,087,736-84,200,632 , GRCh38.p12 chr6: 80,378,019-83,490,913 PGM3, ME1, 24 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
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 RPS27P15, COX7A2, 118 more genes
    nsv6069277insertion1nstd212human GRCh38 chr6: 81,748,552-81,748,552 , GRCh37.p13 chr6: 82,458,269-82,458,269 TENT5A
    nsv6063093insertion1nstd212human GRCh38 chr6: 81,748,605-81,748,605 , GRCh37.p13 chr6: 82,458,322-82,458,322 TENT5A
    nsv5679576mobile element insertion2nstd211human GRCh38 chr6: 81,745,898-81,745,898 , GRCh37.p13 chr6: 82,455,615-82,455,615 TENT5A
    nsv5456635copy number variation1nstd206human GRCh38 chr6: 81,750,162-81,750,837 , GRCh37.p13 chr6: 82,459,879-82,460,554 TENT5A
    nsv5405343mobile element insertion1nstd206human GRCh38 chr6: 81,745,898-81,745,949 , GRCh37.p13 chr6: 82,455,615-82,455,666 TENT5A
    nsv5108874mobile element insertion1nstd203human GRCh38 chr6: 81,745,889-81,745,898 , GRCh37.p13 chr6: 82,455,606-82,455,615 TENT5A
    nsv4945350copy number variation1nstd200human GRCh38 chr6: 81,691,926-82,286,650 , GRCh37.p13 chr6: 82,401,643-82,996,367 , LINC01526, 8 more genes
    nsv4606997copy number variation1nstd183human GRCh37 chr6: 82,455,440-82,455,909 , GRCh38.p12 chr6: 81,745,723-81,746,192 TENT5A
    nsv4479307mobile element insertion1nstd166human GRCh37.p13 chr6: 82,455,606-82,455,606 , GRCh38.p12 chr6: 81,745,889-81,745,889 TENT5A
    nsv4456122copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,216,253-82,753,743 , GRCh38.p12 chr6: 77,506,536-82,044,026 LOC105377869, AK4P5, 38 more genes
    nsv3969115copy number variation1nstd168human GRCh38 chr6: 81,727,690-81,748,434 , GRCh37.p13 chr6: 82,437,407-82,458,151 , TENT5A
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