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Items: 1 to 20 of 62

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973628copy number variation1nstd200human GRCh38 chr10: 51,044,145-51,404,109 , GRCh37.p13 chr10: 52,803,905-53,163,869 PRKG1, MIR605, 2 more genes
    nsv4969954copy number variation1nstd200human GRCh38 chr10: 51,269,223-51,326,789 , GRCh37.p13 chr10: 53,028,983-53,086,549 RSU1P3, PRKG1, 1 more genes
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4455880copy number variation1nstd102humanUncertain significance GRCh37 chr10: 52,082,714-53,320,354 , GRCh38.p12 chr10: 50,322,954-51,560,594 SGMS1, CTSLP4, 16 more genes
    nsv4389374copy number variation1nstd171human GRCh37 chr10: 53,057,466-53,057,500 , GRCh38.p12 chr10: 51,297,706-51,297,740 PRKG1, MIR605
    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
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv3972371copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,390,457-60,061,643 , GRCh38.p12 chr10: 45,931,517-58,301,883 CHAT, CTSLP2, 156 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
    nsv3923539inversion1nstd102humanLikely pathogenic GRCh38.p12 chr10: 43,115,743-59,903,521 , GRCh37 chr10: 43,611,191-61,663,279 ALOX5, CHAT, 248 more genes
    nsv3921181copy number variation1nstd102humanPathogenic NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433 AGAP6, A1CF, 338 more genes
    nsv3917648copy number variation1nstd102humanUncertain significance GRCh37 chr10: 52,727,283-55,468,943 , GRCh38 chr10: 50,967,523-53,709,183 , NCBI36 chr10: 52,397,289-55,138,949 CSTF2T, LOC105378310, 17 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
    nsv3916253copy number variation1nstd102humanPathogenic GRCh38 chr10: 42,884,294-52,265,317 , NCBI36 chr10: 42,699,748-53,695,083 , GRCh37 chr10: 43,379,742-54,025,077 PTPN20CP, ASAH2, 198 more genes
    nsv3909630copy number variation2nstd102humanUncertain significance GRCh37 chr10: 52,085,343-53,314,592 , GRCh38.p12 chr10: 50,325,583-51,554,832 ASAH2B, NUTM2HP, 16 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
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