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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054280inversion1nstd229human GRCh38 chr7: 128,104,928-130,077,832 , GRCh37.p13 chr7: 127,744,980-129,717,672 CICP14, RNA5SP243, 63 more genes
    nsv7054260inversion1nstd229human GRCh38 chr7: 128,247,160-128,264,741 , GRCh37.p13 chr7: 127,887,213-127,904,794 LEP
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7044436inversion1nstd229human GRCh38 chr7: 128,229,837-128,256,394 , GRCh37.p13 chr7: 127,869,890-127,896,447 LEP
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6837532copy number variation1nstd229human GRCh38 chr7: 127,921,601-128,596,800 , GRCh37.p13 chr7: 127,561,654-128,236,854 SND1, MIR129-1, 17 more genes
    nsv6833372copy number variation1nstd229human GRCh38 chr7: 128,256,401-128,264,800 , GRCh37.p13 chr7: 127,896,454-127,904,853 LEP
    nsv6833173copy number variation1nstd229human GRCh38 chr7: 128,204,702-128,251,602 , GRCh37.p13 chr7: 127,844,755-127,891,655 MIR129-1, LEP
    nsv6830429copy number variation1nstd229human GRCh38 chr7: 128,229,801-128,247,200 , GRCh37.p13 chr7: 127,869,854-127,887,253 LEP
    nsv6824252copy number variation1nstd229human GRCh38 chr7: 128,247,703-128,251,449 , GRCh37.p13 chr7: 127,887,756-127,891,502 LEP
    nsv6823536copy number variation1nstd229human GRCh38 chr7: 128,230,852-128,307,165 , GRCh37.p13 chr7: 127,870,905-127,947,218 RBM28, LEP, 1 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
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313722copy number variation1nstd102humanPathogenic GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221 IRF5, MIR129-1, 153 more genes
    nsv6313693copy number variation1nstd102humanUncertain significance GRCh37 chr7: 127,869,902-127,898,641 , GRCh38.p12 chr7: 128,229,849-128,258,588 LEP
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