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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148243copy number variation1nstd102humanPathogenic GRCh38 chr7: 137,463,392-159,345,973 , GRCh37.p13 chr7: 137,148,138-159,128,663 MIR11400, TRBV24-1, 531 more genes
    nsv7148234copy number variation1nstd102humanLikely pathogenic GRCh38 chr7: 138,620,939-159,233,475 , GRCh37.p13 chr7: 138,305,684-159,026,165 AOC1, ALDH7A1P3, 515 more genes
    nsv7097864copy number variation1nstd102humanPathogenic GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959 NOBOX, FAM131B, 466 more genes
    nsv7097607copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr7: 138,391,369-141,759,786 , GRCh38.p12 chr7: 138,706,624-142,059,986 LOC105375535, AGK-DT, 82 more genes
    nsv7057486inversion1nstd229human GRCh38 chr7: 141,032,956-142,024,053 , GRCh37.p13 chr7: 140,732,756-141,557,849 MGAM, LOC105375537, 26 more genes
    nsv7050665inversion1nstd229human GRCh38 chr7: 141,699,336-141,744,043 , GRCh37.p13 chr7: 141,399,136-141,443,843 WEE2-AS1, DENND11, 3 more genes
    nsv7047243inversion1nstd229human GRCh38 chr7: 140,412,248-142,426,166 , GRCh37.p13 chr7: 140,112,048-142,048,195 OR9A4, AGK-DT, 69 more genes
    nsv7044890inversion1nstd229human GRCh38 chr7: 140,412,271-142,426,160 , GRCh37.p13 chr7: 140,112,071-142,048,195 WEE2, LOC105375535, 69 more genes
    nsv7041276inversion1nstd229human GRCh38 chr7: 141,680,649-141,744,044 , GRCh37.p13 chr7: 141,380,449-141,443,844 DENND11, RNU1-82P, 3 more genes
    nsv7040689inversion1nstd229human GRCh38 chr7: 140,412,886-142,426,274 , GRCh37.p13 chr7: 140,112,686-142,048,195 MYL6P4, TMEM178B, 69 more genes
    nsv6830687copy number variation1nstd229human GRCh38 chr7: 141,732,601-141,737,000 , GRCh37.p13 chr7: 141,432,401-141,436,800 WEE2-AS1, SSBP1
    nsv6830253copy number variation1nstd229human GRCh38 chr7: 141,699,060-141,704,449 , GRCh37.p13 chr7: 141,398,860-141,404,249 WEE2-AS1, DENND11
    nsv6826296copy number variation1nstd229human GRCh38 chr7: 141,708,176-141,712,965 , GRCh37.p13 chr7: 141,407,976-141,412,765 WEE2, WEE2-AS1
    nsv6824989copy number variation1nstd229human GRCh38 chr7: 141,643,401-141,709,600 , GRCh37.p13 chr7: 141,343,201-141,409,400 AGK, WEE2-AS1, 2 more genes
    nsv6821788copy number variation1nstd229human GRCh38 chr7: 141,728,601-141,798,500 , GRCh37.p13 chr7: 141,428,401-141,498,300 TAS2R4, WEE2-AS1, 6 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6571546inversion1nstd223human GRCh38 chr7: 141,721,547-141,722,172 , GRCh37.p13 chr7: 141,421,347-141,421,972 WEE2, WEE2-AS1
    nsv6433195copy number variation1nstd223human GRCh38 chr7: 141,713,378-141,715,536 , GRCh37.p13 chr7: 141,413,178-141,415,336 WEE2, WEE2-AS1
    nsv6417232copy number variation1nstd223human GRCh38 chr7: 141,714,720-141,719,001 , GRCh37.p13 chr7: 141,414,520-141,418,801 WEE2-AS1, WEE2
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