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Items: 1 to 20 of 95

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5347812translocation1nstd200human GRCh38 chr10: 68,339,038-68,339,038 , GRCh38 chr10: 68,338,944-68,338,944 , GRCh37.p13 chr10: 70,098,795-70,098,795 , GRCh37.p13 chr10: 70,098,701-70,098,701 HNRNPH3
    nsv5243486copy number variation1nstd204human GRCh38.p13 chr10: 68,209,901-68,601,300 , GRCh37.p13 chr10: 69,969,658-70,361,057 LINC02640, RPL26P27, 12 more genes
    nsv5131847mobile element insertion1nstd203human GRCh38 chr10: 68,334,362-68,334,374 , GRCh37.p13 chr10: 70,094,119-70,094,131 HNRNPH3
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4618563copy number variation1nstd183human GRCh37 chr10: 70,088,504-70,099,035 , GRCh38.p12 chr10: 68,328,747-68,339,278 RUFY2, HNRNPH3, 1 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 MYL6P3, CHCHD1, 220 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 SLC9A3P3, JMJD1C-AS2, 476 more genes
    nsv3912524copy number variation1nstd102humanUncertain significance NCBI36 chr10: 69,617,575-69,763,173 , GRCh37 chr10: 69,947,569-70,093,167 , GRCh38 chr10: 68,187,812-68,333,410 MYPN, PBLD, 4 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3899672copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 68,394,411-70,673,475 , GRCh38.p12 chr10: 66,634,653-68,913,719 DNA2, HNRNPH3, 41 more genes
    nsv3895364copy number variation1nstd102humanBenign GRCh37 chr10: 70,102,749-70,332,271 , GRCh38.p12 chr10: 68,342,992-68,572,514 RUFY2, TMEM14DP, 7 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
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