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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 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
    nsv6824154copy number variation1nstd229human GRCh38 chr7: 131,135,808-131,381,918 , GRCh37.p13 chr7: 130,820,567-131,066,677 RPL27P11, MKLN1, 1 more genes
    nsv6818204copy number variation1nstd229human GRCh38 chr7: 131,260,343-131,518,296 , GRCh37.p13 chr7: 130,945,102-131,203,055 MKLN1-AS, MKLN1, 2 more genes
    nsv6636929copy number variation1nstd102humanUncertain significance GRCh37 chr7: 129,147,455-132,777,678 , GRCh38.p12 chr7: 129,507,614-133,092,918 LINC03008, TMEM209, 60 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
    nsv6561038inversion1nstd223human GRCh38 chr7: 131,325,724-131,326,339 , GRCh37.p13 chr7: 131,010,483-131,011,098 MKLN1, MKLN1-AS
    nsv6560945inversion1nstd223human GRCh38 chr7: 129,758,099-137,582,370 , GRCh37.p13 chr7: 129,397,939-137,267,116 LOC100506937, SLC35B4, 115 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
    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
    nsv6135890copy number variation1nstd213human GRCh37 chr7: 130,930,000-131,300,001 , GRCh38.p12 chr7: 131,245,241-131,615,242 MKLN1, PODXL, 2 more genes
    nsv6135888copy number variation1nstd213human GRCh37 chr7: 130,260,000-136,190,001 , GRCh38.p12 chr7: 130,575,728-136,505,253 AKR1B1, MKLN1, 81 more genes
    nsv5913842copy number variation1nstd209human GRCh38 chr7: 130,970,280-131,332,552 , GRCh37.p13 chr7: 130,721,756-131,017,311 MKLN1, LINC-PINT, 3 more genes
    nsv5848329copy number variation1nstd209human GRCh38 chr7: 131,307,765-131,326,464 , GRCh37.p13 chr7: 130,992,524-131,011,223 MKLN1, MKLN1-AS
    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
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
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