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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4682037copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310 XAB2, CLEC4G, 40 more genes
    nsv4676269copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878 LRRC8E, CLEC4GP1, 47 more genes
    nsv4266162copy number variation1nstd166human GRCh37.p13 chr19: 7,990,116-7,990,167 , GRCh38.p12 chr19: 7,925,231-7,925,282 CTXN1, TIMM44
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 SEMA6B, RANBP3-DT, 299 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
    nsv3900025copy number variation1nstd102humanconflicting data from submitters GRCh37 chr19: 7,989,408-7,990,287 , GRCh38.p12 chr19: 7,924,523-7,925,402 TIMM44, CTXN1
    nsv3890584copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144 PCP2, EIF1P6, 250 more genes
    nsv3165763copy number variation1nstd151human GRCh37 chr19: 7,504,825-8,155,140 , GRCh38.p12 chr19: 7,439,939-8,090,256 SAXO5, LYPLA2P2, 39 more genes
    nsv3165096copy number variation1nstd151human GRCh37 chr19: 7,960,486-8,531,277 , GRCh38.p12 chr19: 7,895,601-8,466,393 RAB11B, FBN3, 22 more genes
    nsv2784211copy number variation1nstd132human NCBI36 chr19: 7,759,053-8,066,334 , GRCh37.p13 chr19: 7,853,053-8,160,334 , GRCh38.p12 chr19: 7,788,167-8,095,450 CTXN1, CLEC4GP1, 14 more genes
    nsv2768220copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 5,092,438-17,933,476 , GRCh37 chr19: 5,092,449-18,044,285 , ACP5, 562 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 , ACP5, 914 more genes
    nsv2768218copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-19,745,645 , GRCh37 chr19: 260,911-19,856,454 , ACP5, 867 more genes
    nsv2768217copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-16,062,156 , GRCh37 chr19: 260,911-16,172,966 , ACP5, 724 more genes
    esv3979717copy number variation3estd229human GRCh37 chr19: 7,987,428-8,000,001 , GRCh38.p12 chr19: 7,922,543-7,935,116 SNAPC2, TIMM44, 1 more genes
    nsv2766848copy number variation1nstd130human NCBI36 chr19: 341,627-8,021,720 , GRCh37.p13 chr19: 390,627-8,115,720 , GRCh38.p12 chr19: 390,627-8,050,836 , TRF-GAA1-6, 335 more genes
    nsv2761227copy number variation1nstd130human GRCh37 chr19: 7,972,827-7,992,126 , GRCh38.p12 chr19: 7,907,942-7,927,241 MAP2K7, TGFBR3L, 3 more genes
    nsv2758626copy number variation1nstd130human GRCh37 chr19: 289,244-19,611,550 , GRCh38.p12 chr19: 289,244-19,500,741 , MAN2B1, 854 more genes
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