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Items: 1 to 20 of 210

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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
    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
    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
    nsv6988636copy number variation1nstd229human GRCh38 chr17: 10,078,018-10,512,683 , GRCh37.p13 chr17: 9,981,335-10,416,000 MYHAS, LOC107985004, 6 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
    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
    nsv6981905copy number variation1nstd229human GRCh38 chr17: 10,507,180-10,508,157 , GRCh37.p13 chr17: 10,410,497-10,411,474 MYH1, MYHAS
    nsv6624535copy number variation5nstd224human GRCh37 chr17: 9,991,587-10,415,842 , GRCh38.p12 chr17: 10,088,270-10,512,525 MYH1, MYH4, 6 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
    nsv6623810copy number variation1nstd224human GRCh37 chr17: 10,003,245-10,415,842 , GRCh38.p12 chr17: 10,099,928-10,512,525 MYH1, MYH4, 6 more genes
    nsv6512317copy number variation1nstd223human GRCh38 chr17: 10,507,167-10,508,162 , GRCh37.p13 chr17: 10,410,484-10,411,479 MYH1, MYHAS
    nsv6503351copy number variation1nstd223human GRCh38 chr17: 10,491,001-10,492,100 , GRCh37.p13 chr17: 10,394,318-10,395,417 MYH1, MYHAS
    nsv6250612mobile element insertion1nstd215human GRCh38 chr17: 10,509,220-10,509,220 , GRCh37.p13 chr17: 10,412,537-10,412,537 MYH1, MYHAS
    nsv6133324copy number variation1nstd213human GRCh37 chr17: 9,930,000-12,980,001 , GRCh38.p12 chr17: 10,026,683-13,076,684 DNAH9, MYH1, 36 more genes
    nsv6112717copy number variation1nstd102humanUncertain significance GRCh38 chr17: 10,078,000-10,512,000 , GRCh37.p13 chr17: 9,981,317-10,415,317 GAS7, MYH8, 6 more genes
    nsv5970150insertion1nstd209human GRCh38 chr17: 10,495,760-10,495,760 , GRCh37.p13 chr17: 10,399,077-10,399,077 MYH1, MYHAS
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