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Items: 1 to 20 of 563

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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
    nsv7097486copy number variation1nstd102humanUncertain significance GRCh37 chr7: 140,624,346-140,624,503 , GRCh38.p12 chr7: 140,924,546-140,924,703 LOC105375536, BRAF
    nsv7097346copy number variation1nstd102humanUncertain significance GRCh37 chr7: 140,534,389-140,534,692 , GRCh38.p12 chr7: 140,834,589-140,834,892 BRAF
    nsv7053153inversion1nstd229human GRCh38 chr7: 140,755,636-140,755,693 , GRCh37.p13 chr7: 140,455,436-140,455,493 BRAF
    nsv7049743inversion1nstd229human GRCh38 chr7: 140,887,105-140,887,177 , GRCh37.p13 chr7: 140,586,905-140,586,977 BRAF
    nsv7047243inversion1nstd229human GRCh38 chr7: 140,412,248-142,426,166 , GRCh37.p13 chr7: 140,112,048-142,048,195 OR9A4, AGK-DT, 69 more genes
    nsv7047167inversion1nstd229human GRCh38 chr7: 140,741,467-140,744,501 , GRCh37.p13 chr7: 140,441,267-140,444,301 BRAF
    nsv7044890inversion1nstd229human GRCh38 chr7: 140,412,271-142,426,160 , GRCh37.p13 chr7: 140,112,071-142,048,195 WEE2, LOC105375535, 69 more genes
    nsv7042004inversion1nstd229human GRCh38 chr7: 140,744,230-140,746,492 , GRCh37.p13 chr7: 140,444,030-140,446,292 BRAF
    nsv7040689inversion1nstd229human GRCh38 chr7: 140,412,886-142,426,274 , GRCh37.p13 chr7: 140,112,686-142,048,195 MYL6P4, TMEM178B, 69 more genes
    nsv6837685copy number variation1nstd229human GRCh38 chr7: 140,815,603-140,823,894 , GRCh37.p13 chr7: 140,515,403-140,523,694 BRAF
    nsv6837309copy number variation1nstd229human GRCh38 chr7: 140,764,001-140,770,600 , GRCh37.p13 chr7: 140,463,801-140,470,400 BRAF
    nsv6837054copy number variation1nstd229human GRCh38 chr7: 140,835,089-140,839,282 , GRCh37.p13 chr7: 140,534,889-140,539,082 BRAF
    nsv6836901copy number variation1nstd229human GRCh38 chr7: 140,908,789-140,909,003 , GRCh37.p13 chr7: 140,608,589-140,608,803 BRAF
    nsv6835977copy number variation1nstd229human GRCh38 chr7: 140,815,384-140,833,162 , GRCh37.p13 chr7: 140,515,184-140,532,962 BRAF
    nsv6835740copy number variation1nstd229human GRCh38 chr7: 140,911,975-140,915,265 , GRCh37.p13 chr7: 140,611,775-140,615,065 BRAF
    nsv6835604copy number variation1nstd229human GRCh38 chr7: 140,839,492-140,844,688 , GRCh37.p13 chr7: 140,539,292-140,544,488 BRAF
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