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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7139923insertion1nstd232human GRCh37.p13 chr4: 56,211,257-56,211,257 , GRCh38.p12 chr4: 55,345,090-55,345,090 SRD5A3
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7049251inversion1nstd229human GRCh38 chr4: 55,354,511-55,354,549 , GRCh37.p13 chr4: 56,220,678-56,220,716 SRD5A3
    nsv7043890inversion1nstd229human GRCh38 chr4: 55,335,201-55,508,922 , GRCh37.p13 chr4: 56,201,368-56,375,089 TMEM165, SRD5A3-AS1, 4 more genes
    nsv6723485copy number variation1nstd229human GRCh38 chr4: 55,332,176-55,534,874 , GRCh37.p13 chr4: 56,198,343-56,401,041 TMEM165, CLOCK, 4 more genes
    nsv6722824copy number variation1nstd229human GRCh38 chr4: 55,358,271-55,363,193 , GRCh37.p13 chr4: 56,224,438-56,229,360 SRD5A3
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6569949inversion1nstd223human GRCh38 chr4: 55,355,855-55,356,024 , GRCh37.p13 chr4: 56,222,022-56,222,191 SRD5A3
    nsv6562250inversion1nstd223human GRCh38 chr4: 55,360,452-55,360,943 , GRCh37.p13 chr4: 56,226,619-56,227,110 SRD5A3
    nsv6389145copy number variation1nstd223human GRCh38 chr4: 55,346,001-55,346,700 , GRCh37.p13 chr4: 56,212,168-56,212,867 SRD5A3
    nsv6315421copy number variation1nstd102humanPathogenic GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280 METTL5P3, RPL38P3, 38 more genes
    nsv6311837copy number variation2nstd102humanUncertain significance GRCh37 chr4: 55,124,936-57,798,318 , GRCh38.p12 chr4: 54,258,769-56,932,152 GLDCP1, KDR, 54 more genes
    nsv6311728copy number variation1nstd102humanPathogenic GRCh37 chr4: 56,225,493-56,225,675 , GRCh38.p12 chr4: 55,359,326-55,359,508 SRD5A3
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6244089mobile element insertion1nstd215human GRCh38 chr4: 55,356,026-55,356,026 , GRCh37.p13 chr4: 56,222,193-56,222,193 SRD5A3
    nsv6135345copy number variation1nstd213human GRCh37 chr4: 55,360,000-63,180,001 , GRCh38.p12 chr4: 54,493,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv6134939copy number variation1nstd213human GRCh37 chr4: 55,330,000-63,180,001 , GRCh38.p12 chr4: 54,463,833-62,314,283 GLDCP1, IGFBP7, 82 more genes
    nsv6071183insertion1nstd212human GRCh38 chr4: 55,360,233-55,360,233 , GRCh37.p13 chr4: 56,226,400-56,226,400 SRD5A3
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