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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095371copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,618,104-79,894,690 , GRCh38.p12 chr17: 81,651,074-81,936,814 CCDC137, PPP1R27, 21 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7069668inversion1nstd229human GRCh38 chr17: 81,803,762-81,809,905 , GRCh37.p13 chr17: 79,761,638-79,767,781 LOC105376789, GCGR
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6274219copy number variation1nstd214human GRCh38 chr17: 81,801,597-81,801,752 , GRCh37.p13 chr17: 79,759,473-79,759,628 LOC105376789
    nsv6204237copy number variation1nstd214human GRCh38 chr17: 81,801,243-81,801,320 , GRCh37.p13 chr17: 79,759,119-79,759,196 LOC105376789
    nsv6193321copy number variation1nstd214human GRCh38 chr17: 81,801,217-81,801,294 , GRCh37.p13 chr17: 79,759,093-79,759,170 LOC105376789
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6035632copy number variation1nstd212human GRCh38 chr17: 81,801,270-81,801,347 , GRCh37.p13 chr17: 79,759,146-79,759,223 LOC105376789
    nsv5946669copy number variation1nstd209human GRCh38 chr17: 81,801,243-81,801,320 , GRCh37.p13 chr17: 79,759,119-79,759,196 LOC105376789
    nsv5887249copy number variation1nstd209human GRCh38 chr17: 81,797,981-81,800,951 , GRCh37.p13 chr: NaN-NaN LOC105376789
    nsv5882115copy number variation1nstd209human GRCh38 chr17: 81,798,315-81,805,253 , GRCh37.p13 chr17: 79,759,050-79,763,129 GCGR, LOC105376789
    nsv5602736copy number variation1nstd207human GRCh38 chr17: 81,801,243-81,801,320 , GRCh37.p13 chr17: 79,759,119-79,759,196 LOC105376789
    nsv5597156copy number variation1nstd207human GRCh38 chr17: 81,798,717-81,798,825 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN LOC105376789
    nsv5363971translocation1nstd200human GRCh38 chr8: 28,576,453-28,576,453 , GRCh38 chr17: 81,799,160-81,799,160 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr8: 28,433,970-28,433,970 LOC105376789
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5290477copy number variation1nstd204human GRCh38.p13 chr17: 81,742,501-82,145,800 , GRCh37.p13 chr17: 79,759,050-80,103,676 PPP1R27, MAFG, 27 more genes
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