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Items: 1 to 20 of 264

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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
    nsv7057176inversion1nstd229human GRCh38 chr7: 142,200,564-149,795,026 , GRCh37.p13 chr7: 141,988,816-149,492,114 RN7SL72P, RPL32P17, 258 more genes
    nsv7046837inversion1nstd229human GRCh38 chr7: 146,996,779-152,901,438 , GRCh37.p13 chr7: 146,693,871-152,598,523 RARRES2, RN7SL76P, 153 more genes
    nsv7046416inversion1nstd229human GRCh38 chr7: 149,665,138-153,434,575 , GRCh37.p13 chr7: 149,362,229-153,131,660 GIMAP1, LOC105375566, 94 more genes
    nsv7044246inversion1nstd229human GRCh38 chr7: 149,704,331-153,494,218 , GRCh37.p13 chr7: 149,401,422-153,191,303 KCNH2, LOC107986858, 93 more genes
    nsv7041414inversion1nstd229human GRCh38 chr7: 149,662,937-152,237,618 , GRCh37.p13 chr7: 149,360,028-151,934,703 GALNTL5, KCNH2, 79 more genes
    nsv7040478inversion1nstd229human GRCh38 chr7: 149,769,203-152,210,377 , GRCh37.p13 chr7: 149,466,292-151,907,462 YBX1P4, ABCF2-H2BK1, 75 more genes
    nsv6831471copy number variation1nstd229human GRCh38 chr7: 149,764,372-149,766,458 , GRCh37.p13 chr7: 149,461,461-149,463,547 ZNF467
    nsv6825983copy number variation1nstd229human GRCh38 chr7: 149,773,968-149,784,358 , GRCh37.p13 chr7: 149,471,057-149,481,446 SSPOP, ZNF467
    nsv6636490copy number variation1nstd102humanPathogenic GRCh37 chr7: 149,332,630-151,498,689 , GRCh38.p12 chr7: 149,635,539-151,801,603 LOC107986858, GIMAP6, 71 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
    nsv6631646copy number variation1nstd224human GRCh37 chr7: 149,430,494-149,463,019 , GRCh38.p12 chr7: 149,733,405-149,765,930 KRBA1, ZNF467
    nsv6631587copy number variation1nstd224human GRCh37 chr7: 149,430,764-149,463,019 , GRCh38.p12 chr7: 149,733,675-149,765,930 KRBA1, ZNF467
    nsv6631586copy number variation3nstd224human GRCh37 chr7: 149,430,347-149,463,019 , GRCh38.p12 chr7: 149,733,258-149,765,930 KRBA1, ZNF467
    nsv6631585copy number variation1nstd224human GRCh37 chr7: 149,331,027-149,488,922 , GRCh38.p12 chr7: 149,633,936-149,791,834 SSPOP, KRBA1, 6 more genes
    nsv6558115inversion1nstd223human GRCh38 chr7: 146,996,771-152,901,398 , GRCh37.p13 chr7: 146,693,863-152,598,483 ZNF398, PRKAG2-AS1, 153 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6315172copy number variation1nstd102humanPathogenic GRCh37 chr7: 149,062,717-159,124,131 , GRCh38.p12 chr7: 149,365,626-159,331,441 KCNH2, SLC4A2, 191 more genes
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