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Items: 1 to 20 of 133

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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
    nsv7055069inversion1nstd229human GRCh38 chr7: 135,149,934-135,160,517 , GRCh37.p13 chr7: 134,834,686-134,845,269 CYREN, TMEM140
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7039626inversion1nstd229human GRCh38 chr7: 135,150,387-135,156,558 , GRCh37.p13 chr7: 134,835,139-134,841,310 CYREN, TMEM140
    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
    nsv6832254copy number variation1nstd229human GRCh38 chr7: 135,151,571-135,219,433 , GRCh37.p13 chr7: 134,836,323-134,904,185 MIR6509, WDR91, 2 more genes
    nsv6832032copy number variation1nstd229human GRCh38 chr7: 135,148,539-135,153,527 , GRCh37.p13 chr7: 134,833,291-134,838,279 CYREN, TMEM140
    nsv6826206copy number variation1nstd229human GRCh38 chr7: 135,132,897-135,467,877 , GRCh37.p13 chr7: 134,817,649-135,152,625 MIR6509, WDR91, 8 more genes
    nsv6636458copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643 TRBD2, TRBV5-2, 403 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
    nsv6560945inversion1nstd223human GRCh38 chr7: 129,758,099-137,582,370 , GRCh37.p13 chr7: 129,397,939-137,267,116 LOC100506937, SLC35B4, 115 more genes
    nsv6423595copy number variation1nstd223human GRCh38 chr7: 135,148,537-135,153,524 , GRCh37.p13 chr7: 134,833,289-134,838,276 CYREN, TMEM140
    nsv6417861copy number variation1nstd223human GRCh38 chr7: 135,151,571-135,219,430 , GRCh37.p13 chr7: 134,836,323-134,904,182 WDR91, TMEM140, 2 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 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
    nsv6290262copy number variation1nstd102humanPathogenic GRCh37 chr7: 133,848,099-145,814,115 , GRCh38.p12 chr7: 134,163,347-146,117,023 TRBJ2-7, PRSS2, 341 more genes
    nsv6136557copy number variation1nstd213human GRCh37 chr7: 134,050,000-138,700,001 , GRCh38.p12 chr7: 134,365,248-139,015,255 AKR1B1, PTN, 68 more genes
    nsv6135966copy number variation1nstd213human GRCh37 chr7: 134,210,000-135,090,001 , GRCh38.p12 chr7: 134,525,248-135,405,249 BPGM, MIR6509, 14 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
    nsv6072305insertion1nstd212human GRCh38 chr7: 135,147,311-135,147,311 , GRCh37.p13 chr7: 134,832,063-134,832,063 CYREN, TMEM140
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