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Items: 1 to 20 of 1595

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112736copy number variation1nstd102humanPathogenic GRCh37 chr10: 48,301,535-51,807,296 , GRCh38.p12 chr10: 45,999,930-49,959,916 SHLD2P3, LOC100420617, 95 more genes
    nsv5969726inversion1nstd209human GRCh38 chr10: 46,314,755-46,382,087 , GRCh37.p13 chr10: 47,685,991-47,746,309 , GRCh37.p13 chr10|NW_003871068.1: 585,870-653,202 ANTXRL, AGAP14P, 2 more genes
    nsv5927175copy number variation1nstd209human GRCh38 chr10: 46,147,857-46,854,246 , GRCh37.p13 chr10|NW_003871068.1: 418,972-1,125,361 , LINC00842, 25 more genes
    nsv5916113copy number variation1nstd209human GRCh38 chr10: 45,791,488-50,132,032 , GRCh37.p13 chr10|NW_003871068.1: 62,603-2,281,126 , GRCh37.p13 chr10: 46,591,857-51,891,792 , LINC02675, 111 more genes
    nsv5914502copy number variation1nstd209human GRCh38 chr10: 45,768,833-50,109,449 , GRCh37.p13 chr10: 46,591,857-51,028,871 , GRCh37.p13 chr10|NW_003871068.1: 39,948-2,281,126 , AGAP13P, 111 more genes
    nsv5910146copy number variation1nstd209human GRCh38 chr10: 46,108,417-47,381,921 , GRCh37.p13 chr10|NW_003871068.1: 379,532-1,653,036 , SYT15, 35 more genes
    nsv5863870copy number variation2nstd209human GRCh38 chr10: 46,357,512-46,360,899 , GRCh37.p13 chr10: 47,728,731-47,732,116 , GRCh37.p13 chr10|NW_003871068.1: 628,627-632,014 AGAP14P
    nsv5489957copy number variation1nstd206human GRCh38 chr10: 46,140,265-46,456,265 , GRCh37.p13 chr10|NW_003871068.1: 411,380-727,380 , GRCh37.p13 chr10: 47,529,171-47,746,309 , HNRNPA1P33, 8 more genes
    nsv5489018copy number variation1nstd206human GRCh38 chr10: 45,680,265-46,362,265 , GRCh37.p13 chr10: 46,224,334-47,733,482 , GRCh37.p13 chr10|NW_003871068.1: 1-633,380 PARGP1-AGAP4, RPL35AP23, 20 more genes
    nsv5380941copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 49,033,586-52,417,694 , GRCh38.p12 chr10: 45,999,930-49,959,916 CHAT, CTSLP2, 95 more genes
    nsv5258563copy number variation1nstd204human GRCh37.p13 chr10|NW_003871068.1: 543,016-695,815 , GRCh37.p13 chr10: 47,643,137-47,746,309 , GRCh38.p13 chr10: 46,271,901-46,424,700 , ANTXRL, 6 more genes
    nsv5258296copy number variation1nstd204human GRCh38.p13 chr10: 46,347,401-46,356,700 , GRCh37.p13 chr10|NW_003871068.1: 618,516-627,815 , GRCh37.p13 chr10: 47,718,630-47,727,926 AGAP14P
    nsv5257199copy number variation1nstd204human GRCh38.p13 chr10: 46,334,801-46,335,400 , GRCh37.p13 chr10: 47,706,037-47,706,631 , GRCh37.p13 chr10|NW_003871068.1: 605,916-606,515 AGAP14P
    nsv5254114copy number variation1nstd204human GRCh38.p13 chr10: 46,350,301-46,351,800 , GRCh37.p13 chr10|NW_003871068.1: 621,416-622,915 , GRCh37.p13 chr10: 47,721,529-47,723,028 AGAP14P
    nsv5253293copy number variation1nstd204human GRCh38.p13 chr10: 46,358,301-46,367,600 , GRCh37.p13 chr10|NW_003871068.1: 629,416-638,715 , GRCh37.p13 chr10: 47,729,520-47,738,817 AGAP14P, FAM25BP
    nsv5252990copy number variation1nstd204human GRCh38.p13 chr10: 46,355,401-46,359,900 , GRCh37.p13 chr10|NW_003871068.1: 626,516-631,015 , GRCh37.p13 chr10: 47,726,629-47,731,117 AGAP14P
    nsv5252776copy number variation1nstd204human GRCh38.p13 chr10: 46,347,401-46,348,100 , GRCh37.p13 chr10|NW_003871068.1: 618,516-619,215 , GRCh37.p13 chr10: 47,718,630-47,719,329 AGAP14P
    nsv5252646copy number variation1nstd204human GRCh38.p13 chr10: 46,337,501-46,338,200 , GRCh37.p13 chr10: 47,708,730-47,709,429 , GRCh37.p13 chr10|NW_003871068.1: 608,616-609,315 AGAP14P
    nsv5252508copy number variation1nstd204human GRCh38.p13 chr10: 46,350,101-46,355,400 , GRCh37.p13 chr10: 47,721,329-47,726,628 , GRCh37.p13 chr10|NW_003871068.1: 621,216-626,515 AGAP14P
    nsv5251502copy number variation1nstd204human GRCh38.p13 chr10: 46,356,359-46,357,511 , GRCh37.p13 chr10: 47,727,585-47,728,730 , GRCh37.p13 chr10|NW_003871068.1: 627,474-628,626 AGAP14P
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