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Items: 1 to 20 of 162

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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
    nsv7052478inversion1nstd229human GRCh38 chr7: 148,598,936-149,120,264 , GRCh37.p13 chr7: 148,296,028-148,817,356 RNY1, CUL1, 16 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
    nsv7040762inversion1nstd229human GRCh38 chr7: 148,598,948-149,120,315 , GRCh37.p13 chr7: 148,296,040-148,817,407 RNU6-650P, COX6B1P1, 16 more genes
    nsv6835367copy number variation1nstd229human GRCh38 chr7: 148,987,014-148,987,115 , GRCh37.p13 chr7: 148,684,106-148,684,207 GHET1, RNY1
    nsv6832993copy number variation1nstd229human GRCh38 chr7: 148,933,698-149,172,239 , GRCh37.p13 chr7: 148,630,790-148,869,331 ZNF398, RNU6-650P, 12 more genes
    nsv6830719copy number variation1nstd229human GRCh38 chr7: 148,977,601-148,992,077 , GRCh37.p13 chr7: 148,674,693-148,689,169 RNY1, RNY3, 1 more genes
    nsv6829861copy number variation1nstd229human GRCh38 chr7: 148,968,442-148,996,456 , GRCh37.p13 chr7: 148,665,534-148,693,548 RNY3, GHET1, 1 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
    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
    nsv6315169copy number variation1nstd102humanPathogenic GRCh37 chr7: 146,927,174-159,128,556 , GRCh38.p12 chr7: 147,230,082-159,335,866 LOC105375554, ATP5PBP3, 233 more genes
    nsv6291241copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,153,261-157,543,640 , GRCh38.p12 chr7: 148,456,169-157,750,948 TRC-GCA23-1, HTR5A-AS1, 210 more genes
    nsv6291163copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,851,002-159,119,707 , GRCh38.p12 chr7: 134,166,250-159,327,017 TRB, ZC3HAV1L, 579 more genes
    nsv6136972copy number variation1nstd213human GRCh37 chr7: 146,490,000-151,820,001 , GRCh38.p12 chr7: 146,792,908-152,122,916 AOC1, KCNH2, 140 more genes
    nsv6135904copy number variation1nstd213human GRCh37 chr7: 148,450,000-150,420,001 , GRCh38.p12 chr7: 148,752,908-150,722,913 EZH2, RNY3, 78 more genes
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