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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093291copy number variation1nstd102humanUncertain significance GRCh38 chr4: 1,804,435-1,804,506 , GRCh37 chr4: 1,806,162-1,806,233 FGFR3
    nsv7096846copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,795,662-1,795,790 , GRCh38.p12 chr4: 1,793,935-1,794,063 FGFR3
    nsv3874961copy number variation1nstd102humanBenign GRCh37 chr4: 1,809,650-1,865,381 , GRCh38.p12 chr4: 1,807,923-1,863,654 FGFR3, LETM1
    nsv3871888copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 1,784,694-1,919,793 , GRCh38.p12 chr4: 1,782,967-1,918,066 FGFR3, LETM1, 2 more genes
    nsv3883962copy number variation1nstd102humanLikely pathogenic GRCh38 chr4: 1,735,761-1,806,926 , GRCh37 chr4: 1,737,488-1,808,653 FGFR3, TACC3, 1 more genes
    nsv3877925copy number variation1nstd102humanBenign GRCh37 chr4: 1,742,616-1,816,281 , GRCh38.p12 chr4: 1,740,889-1,814,554 FGFR3, TACC3, 2 more genes
    nsv3881328copy number variation1nstd102humanBenign GRCh37 chr4: 1,742,616-1,801,241 , GRCh38.p12 chr4: 1,740,889-1,799,514 FGFR3, LOC112268460, 1 more genes
    nsv4728898copy number variation1nstd102humanUncertain significance GRCh37 chr4: 1,778,534-1,912,732 , GRCh38.p12 chr4: 1,776,807-1,911,005 FGFR3, NSD2, 2 more genes
    nsv3885762copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123 FGFR3, CD38, 456 more genes
    nsv3923296copy number variation1nstd102humanPathogenic GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931 FGFR3, OR7E99P, 446 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 FGFR3, USP17L30, 394 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 FGFR3, LOC100421802, 375 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 FGFR3, LOC105374479, 372 more genes
    nsv3915161copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608 FGFR3, CTBP1-AS, 370 more genes
    nsv1398080copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559 FGFR3, RPL10AP7, 366 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 FGFR3, GPR78, 362 more genes
    nsv3915014copy number variation1nstd102humanPathogenic NCBI36 chr4: 75,040-17,097,463 , GRCh38 chr4: 85,149-17,486,742 , GRCh37 chr4: 85,040-17,488,365 FGFR3, LOC100422637, 350 more genes
    nsv3915275copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,447-17,279,636 , GRCh38 chr4: 72,555-17,278,013 , NCBI36 chr4: 62,447-16,888,734 FGFR3, OR7E99P, 347 more genes
    nsv3888069copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760 FGFR3, RPS3AP16, 332 more genes
    nsv3917860copy number variation1nstd102humanPathogenic GRCh38 chr4: 37,335-15,869,056 , NCBI36 chr4: 27,336-15,479,777 , GRCh37 chr4: 37,336-15,870,679 FGFR3, LOC105374338, 330 more genes
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