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Items: 1 to 20 of 113

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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
    nsv7050960inversion1nstd229human GRCh38 chr7: 128,204,462-128,213,285 , GRCh37.p13 chr7: 127,844,515-127,853,338 MIR129-1
    nsv7049925inversion1nstd229human GRCh38 chr7: 128,202,756-128,206,736 , GRCh37.p13 chr7: 127,842,809-127,846,789 MIR129-1
    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
    nsv7046279inversion1nstd229human GRCh38 chr7: 128,206,819-128,206,899 , GRCh37.p13 chr7: 127,846,872-127,846,952 MIR129-1
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    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
    nsv6833173copy number variation1nstd229human GRCh38 chr7: 128,204,702-128,251,602 , GRCh37.p13 chr7: 127,844,755-127,891,655 MIR129-1, LEP
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6562605inversion1nstd223human GRCh38 chr7: 128,202,569-128,206,735 , GRCh37.p13 chr7: 127,842,622-127,846,788 MIR129-1
    nsv6427814copy number variation1nstd223human GRCh38 chr7: 128,206,701-128,209,100 , GRCh37.p13 chr7: 127,846,754-127,849,153 MIR129-1
    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
    nsv6135961copy number variation1nstd213human GRCh37 chr7: 127,140,000-129,720,001 , GRCh38.p12 chr7: 127,499,946-130,080,161 ARF5, FLNC, 74 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
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