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Items: 1 to 20 of 119

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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
    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
    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
    nsv6834878copy number variation1nstd229human GRCh38 chr7: 128,425,401-128,559,700 , GRCh37.p13 chr7: 128,065,455-128,199,754 METTL2B, HILPDA-AS1, 3 more genes
    nsv6832035copy number variation1nstd229human GRCh38 chr7: 128,354,799-128,479,739 , GRCh37.p13 chr7: 127,994,853-128,119,793 IMPDH1, HILPDA-AS1, 6 more genes
    nsv6822658copy number variation1nstd229human GRCh38 chr7: 128,433,103-128,569,299 , GRCh37.p13 chr7: 128,073,157-128,209,353 RPS10P15, RPL37P16, 4 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
    nsv6290831copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,024,806-128,373,998 , GRCh38.p12 chr7: 128,384,752-128,733,944 RNA5SP242, IMP3P2, 14 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
    nsv6135554copy number variation1nstd213human GRCh37 chr7: 126,190,000-130,150,001 , GRCh38.p12 chr7: 126,549,946-130,510,160 IMPDH1, ODCP, 96 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
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