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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146366insertion1nstd232human GRCh37.p13 chr5: 65,455,162-65,455,162 , GRCh38.p12 chr5: 66,159,334-66,159,334 SREK1
    nsv7056727inversion1nstd229human GRCh38 chr5: 66,154,043-66,154,091 , GRCh37.p13 chr5: 65,449,871-65,449,919 SREK1
    nsv7056369inversion1nstd229human GRCh38 chr5: 65,805,475-66,519,014 , GRCh37.p13 chr5: 65,101,302-65,814,842 SREK1, LOC105379004, 7 more genes
    nsv6773078copy number variation1nstd229human GRCh38 chr5: 66,181,489-66,188,261 , GRCh37.p13 chr5: 65,477,317-65,484,089 SREK1
    nsv6765997copy number variation1nstd229human GRCh38 chr5: 66,182,824-66,190,252 , GRCh37.p13 chr5: 65,478,652-65,486,080 SREK1
    nsv6765534copy number variation1nstd229human GRCh38 chr5: 66,152,401-66,522,200 , GRCh37.p13 chr5: 65,448,229-65,818,028 LOC105379004, LOC105379002, 4 more genes
    nsv6761252copy number variation1nstd229human GRCh38 chr5: 66,107,004-66,145,362 , GRCh37.p13 chr5: 65,402,832-65,441,190 SREK1
    nsv6760692copy number variation1nstd229human GRCh38 chr5: 66,174,155-66,174,267 , GRCh37.p13 chr5: 65,469,983-65,470,095 SREK1
    nsv6759567copy number variation1nstd229human GRCh38 chr5: 66,147,854-66,148,357 , GRCh37.p13 chr5: 65,443,682-65,444,185 SREK1
    nsv6636810copy number variation1nstd102humanUncertain significance GRCh37 chr5: 65,445,482-65,714,525 , GRCh38.p12 chr5: 66,149,654-66,418,697 LINC02065, LOC105379003, 2 more genes
    nsv6411637copy number variation1nstd223human GRCh38 chr5: 66,179,664-66,180,370 , GRCh37.p13 chr5: 65,475,492-65,476,198 SREK1
    nsv6411357copy number variation1nstd223human GRCh38 chr5: 66,179,328-66,255,938 , GRCh37.p13 chr5: 65,475,156-65,551,766 LINC02065, SREK1
    nsv6409084copy number variation1nstd223human GRCh38 chr5: 66,180,585-66,181,013 , GRCh37.p13 chr5: 65,476,413-65,476,841 SREK1
    nsv6408391copy number variation1nstd223human GRCh38 chr5: 66,147,832-66,148,368 , GRCh37.p13 chr5: 65,443,660-65,444,196 SREK1
    nsv6407985copy number variation1nstd223human GRCh38 chr5: 66,170,690-66,171,309 , GRCh37.p13 chr5: 65,466,518-65,467,137 SREK1
    nsv6403354copy number variation1nstd223human GRCh38 chr5: 66,156,501-66,158,400 , GRCh37.p13 chr5: 65,452,329-65,454,228 SREK1
    nsv6401479copy number variation1nstd223human GRCh38 chr5: 66,181,489-66,188,255 , GRCh37.p13 chr5: 65,477,317-65,484,083 SREK1
    nsv6400113copy number variation1nstd223human GRCh38 chr5: 66,173,201-66,174,300 , GRCh37.p13 chr5: 65,469,029-65,470,128 SREK1
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6136128copy number variation1nstd213human GRCh37 chr5: 62,820,000-66,080,001 , GRCh38.p12 chr5: 63,524,173-66,784,173 TRIM23, HTR1A, 33 more genes
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