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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5027506copy number variation1nstd200human GRCh38 chr19: 6,741,539-6,751,287 , GRCh37.p13 chr19: 6,741,550-6,751,298 , TRIP10, 1 more genes
    nsv4852792copy number variation1nstd200human GRCh37 chr19: 6,741,550-6,751,298 , GRCh38.p12 chr19: 6,741,539-6,751,287 , SH2D3A, 1 more genes
    nsv4676363copy number variation1nstd102humanUncertain significance GRCh37 chr19: 6,246,138-6,823,741 , GRCh38.p12 chr19: 6,246,127-6,823,730 SLC25A23, PSPN, 26 more genes
    nsv4626041copy number variation1nstd183human GRCh37 chr19: 6,736,898-6,741,149 , GRCh38.p12 chr19: 6,736,887-6,741,138 MIR6791, TRIP10, 1 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 POLR2E, PWWP3A, 283 more genes
    nsv3918411copy number variation1nstd102humanUncertain significance GRCh38 chr19: 5,905,175-6,916,287 , GRCh37 chr19: 5,905,186-6,916,298 , NCBI36 chr19: 5,856,186-6,867,298 CAPS, MIR6790, 36 more genes
    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
    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
    nsv3166810copy number variation1nstd151human GRCh37 chr19: 6,742,975-6,750,447 , GRCh38.p12 chr19: 6,742,964-6,750,436 , TRIP10, 1 more genes
    nsv3163404copy number variation1nstd151human GRCh37 chr19: 6,739,770-6,739,801 , GRCh38.p12 chr19: 6,739,759-6,739,790 TRIP10
    nsv3162161copy number variation1nstd151human GRCh37 chr19: 6,710,647-6,940,045 , GRCh38.p12 chr19: 6,710,636-6,940,034 , MIR6791, 7 more genes
    nsv3161977copy number variation1nstd151human GRCh37 chr19: 6,718,102-6,773,027 , GRCh38.p12 chr19: 6,718,091-6,773,016 , C3, 5 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
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