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Items: 1 to 20 of 187

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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
    nsv7148154copy number variation1nstd102humanPathogenic GRCh38 chr7: 154,446,117-159,206,757 , GRCh37.p13 chr7: 154,143,202-158,999,446 LOC105375602, LOC105375599, 70 more genes
    nsv7097356copy number variation2nstd102humanPathogenic GRCh37 chr7: 152,617,597-158,500,659 , GRCh38.p12 chr7: 152,920,512-158,707,968 LOC107986722, LOC105375593, 76 more genes
    nsv7073853inversion1nstd229human GRCh38 chr7: 157,262,180-158,244,897 , GRCh37.p13 chr7: 157,054,874-158,037,589 UBE3C, LOC105375614, 9 more genes
    nsv6836439copy number variation1nstd229human GRCh38 chr7: 157,409,626-157,912,835 , GRCh37.p13 chr7: 157,202,320-157,705,527 LOC105375614, LOC105375615, 6 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
    nsv6562942inversion1nstd223human GRCh38 chr7: 157,375,919-158,261,000 , GRCh37.p13 chr7: 157,168,613-158,053,692 PTPRN2, DNAJB6, 7 more genes
    nsv6315450copy number variation1nstd102humanPathogenic GRCh37 chr7: 155,389,460-157,960,969 , GRCh38.p12 chr7: 155,596,766-158,168,277 RNF32, MIR153-2, 38 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
    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
    nsv6290897copy number variation1nstd102humanPathogenic GRCh37 chr7: 148,695,373-159,119,707 , GRCh38.p12 chr7: 148,998,281-159,327,017 TRC-GCA21-1, LINC00996, 209 more genes
    nsv6136980copy number variation1nstd213human GRCh37 chr7: 157,210,000-157,410,001 , GRCh38.p12 chr7: 157,417,306-157,617,309 PTPRN2, DNAJB6, 5 more genes
    nsv6136978copy number variation1nstd213human GRCh37 chr7: 156,250,000-159,138,663 , GRCh38.p12 chr7: 156,457,306-159,335,973 MNX1, PTPRN2, 39 more genes
    nsv6136977copy number variation1nstd213human GRCh37 chr7: 155,830,000-159,138,663 , GRCh38.p12 chr7: 156,037,306-159,335,973 DNAJB6, LMBR1, 44 more genes
    nsv6135980copy number variation1nstd213human GRCh37 chr7: 154,380,000-159,138,663 , GRCh38.p12 chr7: 154,588,290-159,335,973 DPP6, INSIG1, 71 more genes
    nsv6135908copy number variation1nstd213human GRCh37 chr7: 154,510,000-159,138,663 , GRCh38.p12 chr7: 154,718,290-159,335,973 EN2, VIPR2, 70 more genes
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