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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147988insertion1nstd232human GRCh37.p13 chr6: 1,054,055-1,054,055 , GRCh38.p12 chr6: 1,053,820-1,053,820 LINC01622
    nsv7141279insertion1nstd232human GRCh37.p13 chr6: 1,051,972-1,051,972 , GRCh38.p12 chr6: 1,051,737-1,051,737 LINC01622
    nsv7137073copy number variation1nstd102humanPathogenic GRCh37 chr6: 491,126-1,624,775 , GRCh38.p12 chr6: 491,126-1,624,540 RN7SL352P, LOC107986555, 18 more genes
    nsv7137049copy number variation1nstd102humanPathogenic GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531 LOC105374883, LINC02525, 57 more genes
    nsv7093363copy number variation1nstd102humanPathogenic GRCh37 chr6: 820,000-21,700,000 , GRCh38.p12 chr6: 820,000-21,699,769 LOC101928354, CNN3P1, 321 more genes
    nsv7038346inversion1nstd229human GRCh38 chr6: 963,870-967,316 , GRCh37.p13 chr6: 964,109-967,555 LINC01622
    nsv6797883copy number variation1nstd229human GRCh38 chr6: 767,683-1,245,131 , GRCh37.p13 chr6: 767,683-1,245,366 LINC01622, LOC101927691
    nsv6797875copy number variation1nstd229human GRCh38 chr6: 992,800-1,017,712 , GRCh37.p13 chr6: 993,035-1,017,947 LINC01622
    nsv6797846copy number variation1nstd229human GRCh38 chr6: 1,018,714-1,019,075 , GRCh37.p13 chr6: 1,018,949-1,019,310 LINC01622
    nsv6797836copy number variation1nstd229human GRCh38 chr6: 913,022-1,109,920 , GRCh37.p13 chr6: 913,272-1,110,155 LINC01622
    nsv6797217copy number variation1nstd229human GRCh38 chr6: 974,748-984,501 , GRCh37.p13 chr6: 974,984-984,736 LINC01622
    nsv6795796copy number variation1nstd229human GRCh38 chr6: 1,101,176-1,105,142 , GRCh37.p13 chr6: 1,101,411-1,105,377 LINC01622
    nsv6795449copy number variation1nstd229human GRCh38 chr6: 859,377-1,289,626 , GRCh37.p13 chr6: 859,377-1,289,861 LINC01622, LOC105374879, 1 more genes
    nsv6794514copy number variation1nstd229human GRCh38 chr6: 1,013,382-1,013,399 , GRCh37.p13 chr6: 1,013,617-1,013,634 LINC01622
    nsv6793918copy number variation1nstd229human GRCh38 chr6: 1,053,749-1,067,518 , GRCh37.p13 chr6: 1,053,984-1,067,753 LINC01622
    nsv6792464copy number variation1nstd229human GRCh38 chr6: 952,253-977,551 , GRCh37.p13 chr6: 952,494-977,790 LINC01622
    nsv6791703copy number variation1nstd229human GRCh38 chr6: 1,007,116-1,007,875 , GRCh37.p13 chr6: 1,007,351-1,008,110 LINC01622
    nsv6791196copy number variation1nstd229human GRCh38 chr6: 979,423-987,284 , GRCh37.p13 chr6: 979,661-987,519 LINC01622
    nsv6790647copy number variation1nstd229human GRCh38 chr6: 939,761-1,073,796 , GRCh37.p13 chr6: 940,009-1,074,031 LINC01622
    nsv6790205copy number variation1nstd229human GRCh38 chr6: 1,037,076-1,307,142 , GRCh37.p13 chr6: 1,037,311-1,307,377 LOC105374879, LINC01622
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