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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5483515copy number variation1nstd206human GRCh38 chr10: 47,586,000-50,754,368 , GRCh37.p13 chr10: 46,591,857-52,514,128 HMGB1P50, PARG, 65 more genes
    nsv5251416copy number variation1nstd204human GRCh38.p13 chr10: 50,563,464-50,607,083 , GRCh37.p13 chr10: 52,323,224-52,366,843 SGMS1, RNU7-107P
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4973623copy number variation1nstd200human GRCh38 chr10: 50,403,550-50,651,629 , GRCh37.p13 chr10: 52,163,310-52,411,389 RNU7-107P, SHQ1P1, 2 more genes
    nsv4969939copy number variation1nstd200human GRCh38 chr10: 50,560,783-50,589,207 , GRCh37.p13 chr10: 52,320,543-52,348,967 SGMS1, RNU7-107P
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4846254copy number variation1nstd200human GRCh37 chr10: 52,163,310-52,411,389 , GRCh38.p12 chr10: 50,403,550-50,651,629 SHQ1P1, RNU7-107P, 2 more genes
    nsv4834523copy number variation1nstd200human GRCh37 chr10: 52,320,543-52,348,967 , GRCh38.p12 chr10: 50,560,783-50,589,207 RNU7-107P, SGMS1
    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
    nsv4675379copy number variation1nstd102humanUncertain significance GRCh37 chr10: 51,659,413-52,476,136 , GRCh38.p12 chr10: 49,959,917-50,716,376 TIMM23B-AGAP6, NUTM2HP, 18 more genes
    nsv4615421copy number variation1nstd183human GRCh37 chr10: 51,635,623-52,451,272 , GRCh38.p12 chr10: 49,959,917-50,691,512 SLC9A3P1, ASAH2, 15 more genes
    nsv4456736copy number variation1nstd102humanUncertain significance GRCh37 chr10: 51,744,546-52,428,369 , GRCh38.p12 chr10: 49,984,786-50,668,609 ASAH2, FAM21EP, 12 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
    nsv4373606copy number variation1nstd173human GRCh37 chr10: 51,751,180-52,476,136 , GRCh38.p12 chr10: 49,991,420-50,716,376 SHQ1P1, RNU7-107P, 16 more genes
    nsv4366250copy number variation1nstd173human GRCh37 chr10: 51,720,449-52,476,136 , GRCh38.p12 chr10: 49,960,706-50,716,376 TIMM23B-AGAP6, NUTM2HP, 18 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
    nsv4313384inversion1nstd166human GRCh37.p13 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , RET, 306 more genes
    nsv4181825copy number variation1nstd166human GRCh37.p13 chr10: 52,320,543-52,348,967 , GRCh38.p12 chr10: 50,560,783-50,589,207 SGMS1, RNU7-107P
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