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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
    nsv7147739copy number variation1nstd232human GRCh37.p13 chr6: 42,986,903-42,987,024 , GRCh38.p12 chr6: 43,019,165-43,019,286 KLHDC3
    nsv7140562copy number variation1nstd232human GRCh37.p13 chr6: 42,980,765-42,980,850 , GRCh38.p12 chr6: 43,013,027-43,013,112 MEA1, KLHDC3
    nsv7137488copy number variation1nstd232human GRCh37.p13 chr6: 42,986,294-42,986,369 , GRCh38.p12 chr6: 43,018,556-43,018,631 KLHDC3
    nsv7097826copy number variation1nstd102humanPathogenic GRCh37 chr6: 41,126,341-43,752,536 , GRCh38.p12 chr6: 41,158,603-43,784,799 USP49, PRICKLE4, 96 more genes
    nsv7097825copy number variation1nstd102humanUncertain significance GRCh37 chr6: 41,126,341-43,737,486 , GRCh38.p12 chr6: 41,158,603-43,769,749 DNPH1, LOC107986596, 96 more genes
    nsv7097331copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,162,409-44,154,249 , GRCh38.p12 chr6: 42,194,671-44,186,512 MRPS10, CUL9, 70 more genes
    nsv7043293inversion1nstd229human GRCh38 chr6: 39,854,165-43,261,822 , GRCh37.p13 chr6: 39,821,941-43,229,560 RPL23P6, RPL32P15, 95 more genes
    nsv6793691copy number variation1nstd229human GRCh38 chr6: 43,015,722-43,023,433 , GRCh37.p13 chr6: 42,983,460-42,991,171 RRP36, MEA1, 1 more genes
    nsv6792679copy number variation1nstd229human GRCh38 chr6: 42,936,101-43,096,800 , GRCh37.p13 chr6: 42,903,839-43,064,538 PEX6, KLC4, 13 more genes
    nsv6791704copy number variation1nstd229human GRCh38 chr6: 42,737,001-44,115,000 , GRCh37.p13 chr6: 42,704,739-44,082,737 ZNF318, RPL24P4, 56 more genes
    nsv6788702copy number variation1nstd229human GRCh38 chr6: 42,518,401-43,332,100 , GRCh37.p13 chr6: 42,486,139-43,299,838 DNPH1, MRPL2, 31 more genes
    nsv6785753copy number variation1nstd229human GRCh38 chr6: 42,646,801-43,317,300 , GRCh37.p13 chr6: 42,614,539-43,285,038 KLHDC3, CNPY3-GNMT, 30 more genes
    nsv6566770inversion1nstd223human GRCh38 chr6: 42,194,666-44,186,502 , GRCh37.p13 chr6: 42,162,404-44,154,239 RPL36AP5, MIR6780B, 70 more genes
    nsv6557446inversion1nstd223human GRCh38 chr6: 43,015,605-43,016,052 , GRCh37.p13 chr6: 42,983,343-42,983,790 MEA1, KLHDC3
    nsv6290908copy number variation1nstd102humanUncertain significance GRCh37 chr6: 42,548,155-43,053,728 , GRCh38.p12 chr6: 42,580,417-43,085,990 GNMT, CUL7, 23 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5899267copy number variation1nstd209human GRCh38 chr6: 42,957,850-43,031,425 , GRCh37.p13 chr6: 42,925,588-42,999,163 MEA1, PEX6, 5 more genes
    nsv5845514copy number variation1nstd209human GRCh38 chr6: 43,006,921-43,029,742 , GRCh37.p13 chr6: 42,974,659-42,997,480 MEA1, PPP2R5D, 2 more genes
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
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