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Items: 1 to 20 of 179

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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
    nsv7140303insertion1nstd232human GRCh37.p13 chr17: 10,584,571-10,584,571 , GRCh38.p12 chr17: 10,681,254-10,681,254 SCO1
    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
    nsv6996786copy number variation1nstd229human GRCh38 chr17: 10,688,818-10,689,134 , GRCh37.p13 chr17: 10,592,135-10,592,451 SCO1
    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
    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
    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
    nsv6984223copy number variation1nstd229human GRCh38 chr17: 10,671,701-10,683,300 , GRCh37.p13 chr17: 10,575,018-10,586,617 SCO1, MYH3
    nsv6979538copy number variation1nstd229human GRCh38 chr17: 10,663,855-10,679,956 , GRCh37.p13 chr17: 10,567,172-10,583,273 MYH3, SCO1
    nsv6978875copy number variation1nstd229human GRCh38 chr17: 10,662,487-10,685,982 , GRCh37.p13 chr17: 10,565,804-10,589,299 MYH3, SCO1
    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
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