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Items: 1 to 20 of 195

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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
    nsv7072074inversion1nstd229human GRCh38 chr17: 10,322,193-11,492,057 , GRCh37.p13 chr17: 10,225,510-11,395,374 ADPRM, MYH4, 18 more genes
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    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
    nsv6994706copy number variation1nstd229human GRCh38 chr17: 10,547,282-10,563,211 , GRCh37.p13 chr17: 10,450,599-10,466,528 MYH2, MYHAS
    nsv6989889copy number variation1nstd229human GRCh38 chr17: 10,314,520-10,737,161 , GRCh37.p13 chr17: 10,217,837-10,640,478 MYH3, MAGOH2P, 11 more genes
    nsv6989092copy number variation1nstd229human GRCh38 chr17: 10,322,350-10,944,267 , GRCh37.p13 chr17: 10,225,667-10,847,584 LOC105371536, MYH4, 16 more genes
    nsv6988573copy number variation1nstd229human GRCh38 chr17: 10,067,767-10,534,575 , GRCh37.p13 chr17: 9,971,084-10,437,892 MYH8, GAS7, 7 more genes
    nsv6987986copy number variation1nstd229human GRCh38 chr17: 10,184,262-10,772,232 , GRCh37.p13 chr17: 10,087,579-10,675,549 MYH2, MYH8, 13 more genes
    nsv6986876copy number variation1nstd229human GRCh38 chr17: 10,522,412-10,569,990 , GRCh37.p13 chr17: 10,425,729-10,473,307 MYHAS, MYH2
    nsv6985321copy number variation1nstd229human GRCh38 chr17: 10,044,227-10,676,131 , GRCh37.p13 chr17: 9,947,544-10,579,448 MYH4, MYH1, 9 more genes
    nsv6624196copy number variation1nstd224human GRCh37 chr17: 10,402,754-10,432,735 , GRCh38.p12 chr17: 10,499,437-10,529,418 MYH1, MYHAS, 1 more genes
    nsv6314458insertion1nstd102humanPathogenic GRCh37 chr17: 10,438,674-10,438,674 , GRCh38 chr17: 10,535,357-10,535,357 MYH2, MYHAS
    nsv6310051copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,432,459-10,433,077 , GRCh38.p12 chr17: 10,529,142-10,529,760 MYHAS, MYH2
    nsv6310050copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 10,432,333-10,434,433 , GRCh38.p12 chr17: 10,529,016-10,531,116 MYH2, MYHAS
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