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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7040227inversion1nstd229human GRCh38 chr4: 38,679,217-38,688,413 , GRCh37.p13 chr4: 38,680,838-38,690,034 KLF3
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6736257copy number variation1nstd229human GRCh38 chr4: 38,681,409-38,684,480 , GRCh37.p13 chr4: 38,683,030-38,686,101 KLF3
    nsv6735771copy number variation1nstd229human GRCh38 chr4: 38,683,177-38,686,556 , GRCh37.p13 chr4: 38,684,798-38,688,177 KLF3
    nsv6724485copy number variation1nstd229human GRCh38 chr4: 38,667,351-38,668,046 , GRCh37.p13 chr4: 38,668,972-38,669,667 KLF3
    nsv6720211copy number variation1nstd229human GRCh38 chr4: 38,662,721-38,662,807 , GRCh37.p13 chr4: 38,664,342-38,664,428 KLF3-AS1, KLF3
    nsv6720085copy number variation1nstd229human GRCh38 chr4: 38,701,501-39,003,800 , GRCh37.p13 chr4: 38,703,122-39,005,420 TLR1, LOC105374413, 7 more genes
    nsv6636898copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,589,565-38,926,476 , GRCh38.p12 chr4: 38,587,944-38,924,855 TLR10, MIR574, 7 more genes
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6569233inversion1nstd223human GRCh38 chr4: 38,680,303-38,680,938 , GRCh37.p13 chr4: 38,681,924-38,682,559 KLF3
    nsv6388961copy number variation1nstd223human GRCh38 chr4: 38,690,684-38,691,287 , GRCh37.p13 chr4: 38,692,305-38,692,908 KLF3
    nsv6315440copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552 FAM86KP, ENPP7P11, 631 more genes
    nsv6291155copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,459,610-38,724,190 , GRCh38.p12 chr4: 38,457,989-38,722,569 LINC01258, KLF3-AS1, 3 more genes
    nsv6135584copy number variation1nstd213human GRCh37 chr4: 38,420,000-39,480,001 , GRCh38.p12 chr4: 38,418,379-39,478,381 RFC1, RPL9, 22 more genes
    nsv5997183copy number variation1nstd212human GRCh38 chr4: 38,663,479-38,663,552 , GRCh37.p13 chr4: 38,665,100-38,665,173 KLF3-AS1, KLF3
    nsv5889240copy number variation1nstd209human GRCh38 chr4: 38,479,825-38,850,299 , GRCh37.p13 chr4: 38,481,446-38,851,920 , KLF3, 10 more genes
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