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Items: 1 to 20 of 64

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875451copy number variation1nstd102humanBenign GRCh37 chr4: 13,377,286-13,391,279 , GRCh38.p12 chr4: 13,375,662-13,389,655 RAB28
    nsv3874215copy number variation1nstd102humanBenign GRCh37 chr4: 13,377,286-13,381,870 , GRCh38.p12 chr4: 13,375,662-13,380,246 RAB28
    nsv3871057copy number variation1nstd102humanBenign GRCh37 chr4: 13,380,921-13,381,870 , GRCh38.p12 chr4: 13,379,297-13,380,246 RAB28
    nsv6311824copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,475,922-13,476,050 , GRCh38.p12 chr4: 13,474,298-13,474,426 RAB28
    nsv6311823copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,371,500-13,383,238 , GRCh38.p12 chr4: 13,369,876-13,381,614 RAB28
    nsv7096981copy number variation1nstd102humanUncertain significance GRCh37 chr4: 13,371,500-13,546,038 , GRCh38.p12 chr4: 13,369,876-13,544,414 RAB28, LINC01097, 3 more genes
    nsv3877950copy number variation1nstd102humanPathogenic GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159 RAB28, LOC100418700, 353 more genes
    nsv3885762copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123 RAB28, 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 RAB28, OR7E99P, 446 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 RAB28, LOC105374542, 232 more genes
    nsv4674378copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859 RAB28, USP17L30, 394 more genes
    nsv6315347copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952 RAB28, LOC100421802, 375 more genes
    nsv6291097copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544 RAB28, 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 RAB28, CTBP1-AS, 370 more genes
    nsv1398080copy number variation1nstd102humanPathogenic GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559 RAB28, RPL10AP7, 366 more genes
    nsv6112747copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372 RAB28, 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 RAB28, 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 RAB28, OR7E99P, 347 more genes
    nsv3888069copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760 RAB28, 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 RAB28, LOC105374338, 330 more genes
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