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Items: 1 to 20 of 771

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7095073copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,436,582-10,600,824 , GRCh38.p12 chr17: 10,533,265-10,697,507 MYH3, ADPRM, 3 more genes
    nsv7095072copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,424,597-10,433,077 , GRCh38.p12 chr17: 10,521,280-10,529,760 MYH2, MYHAS
    nsv7095071copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,424,597-10,431,211 , GRCh38.p12 chr17: 10,521,280-10,527,894 MYHAS, MYH2
    nsv7094953copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,432,861-10,433,411 , GRCh38.p12 chr17: 10,529,544-10,530,094 MYHAS, MYH2
    nsv7094952copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,424,597-10,433,411 , GRCh38.p12 chr17: 10,521,280-10,530,094 MYH2, MYHAS
    nsv7094623copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 10,501,075-10,554,989 , GRCh38.p12 chr17: 10,597,758-10,651,672 MYH3, MYHAS
    nsv7077400inversion1nstd229human GRCh38 chr17: 10,453,981-10,458,166 , GRCh37.p13 chr17: 10,357,298-10,361,483 MYHAS, MYH4
    nsv7072074inversion1nstd229human GRCh38 chr17: 10,322,193-11,492,057 , GRCh37.p13 chr17: 10,225,510-11,395,374 ADPRM, MYH4, 18 more genes
    nsv7068964inversion1nstd229human GRCh38 chr17: 10,443,856-10,458,286 , GRCh37.p13 chr17: 10,347,173-10,361,603 MYHAS, MYH4
    nsv7065106inversion1nstd229human GRCh38 chr17: 10,475,811-10,475,956 , GRCh37.p13 chr17: 10,379,128-10,379,273 MYHAS
    nsv7064039inversion1nstd229human GRCh38 chr17: 10,619,043-10,650,289 , GRCh37.p13 chr17: 10,522,360-10,553,606 MYHAS, MYH3
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv7062936inversion1nstd229human GRCh38 chr17: 10,597,758-10,651,672 , GRCh37.p13 chr17: 10,501,075-10,554,989 MYH3, MYHAS
    nsv7060032inversion1nstd229human GRCh38 chr17: 10,568,496-10,568,555 , GRCh37.p13 chr17: 10,471,813-10,471,872 MYHAS
    nsv6997035copy number variation1nstd229human GRCh38 chr17: 9,981,556-11,548,056 , GRCh37.p13 chr17: 9,884,873-11,451,373 LOC107985004, MYH2, 20 more genes
    nsv6997009copy number variation1nstd229human GRCh38 chr17: 10,555,346-10,557,718 , GRCh37.p13 chr17: 10,458,663-10,461,035 MYHAS
    nsv6996660copy number variation1nstd229human GRCh38 chr17: 10,606,310-10,712,067 , GRCh37.p13 chr17: 10,509,627-10,615,384 TMEM220, SCO1, 3 more genes
    nsv6995674copy number variation1nstd229human GRCh38 chr17: 10,464,374-10,466,730 , GRCh37.p13 chr17: 10,367,691-10,370,047 MYH4, MYHAS
    nsv6995083copy number variation1nstd229human GRCh38 chr17: 10,469,501-10,483,000 , GRCh37.p13 chr17: 10,372,818-10,386,317 MYH4, MYHAS
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