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Items: 1 to 20 of 161

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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
    nsv7095074copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,531,970-10,600,824 , GRCh38.p12 chr17: 10,628,653-10,697,507 ADPRM, SCO1, 1 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
    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
    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
    nsv6995870copy number variation1nstd229human GRCh38 chr17: 10,706,132-10,709,809 , GRCh37.p13 chr17: 10,609,449-10,613,126 TMEM220, ADPRM
    nsv6993743copy number variation1nstd229human GRCh38 chr17: 10,658,774-11,321,014 , GRCh37.p13 chr17: 10,562,091-11,224,331 MYH3, SCO1, 11 more genes
    nsv6993504copy number variation1nstd229human GRCh38 chr17: 10,690,924-10,747,710 , GRCh37.p13 chr17: 10,594,241-10,651,027 ADPRM, TMEM220, 3 more genes
    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
    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
    nsv6982333copy number variation1nstd229human GRCh38 chr17: 10,701,591-10,703,220 , GRCh37.p13 chr17: 10,604,908-10,606,537 ADPRM
    nsv6638024copy number variation1nstd102humanUncertain significance GRCh37 chr17: 10,517,286-10,814,075 , GRCh38.p12 chr17: 10,613,969-10,910,758 SCO1, TMEM220-AS1, 10 more genes
    nsv6584597inversion1nstd223human GRCh38 chr17: 10,695,462-10,696,845 , GRCh37.p13 chr17: 10,598,779-10,600,162 ADPRM, SCO1
    nsv6506694copy number variation1nstd223human GRCh38 chr17: 10,615,797-10,787,245 , GRCh37.p13 chr17: 10,519,114-10,690,562 MYH3, TMEM220-AS1, 5 more genes
    nsv6500836copy number variation1nstd223human GRCh38 chr17: 10,606,310-10,712,065 , GRCh37.p13 chr17: 10,509,627-10,615,382 TMEM220, MYH3, 3 more genes
    nsv6498306copy number variation1nstd223human GRCh38 chr17: 10,711,037-10,713,200 , GRCh37.p13 chr17: 10,614,354-10,616,517 ADPRM, TMEM220
    nsv6497937copy number variation1nstd223human GRCh38 chr17: 10,704,601-10,710,000 , GRCh37.p13 chr17: 10,607,918-10,613,317 TMEM220, ADPRM
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