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Items: 1 to 20 of 2626

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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
    nsv5967347insertion1nstd209human GRCh38 chr10: 47,743,327-47,743,327 , GRCh37.p13 chr: NaN-NaN ANXA8, SYT15B, 1 more genes
    nsv5958705insertion1nstd209human GRCh38 chr10: 47,962,671-47,962,671 , GRCh37.p13 chr10|NW_003871068.1: 2,152,567-2,152,567 ANXA8
    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
    nsv5915610copy number variation1nstd209human GRCh38 chr10: 47,733,151-47,733,232 , GRCh37.p13 chr10|NW_003871068.1: 2,004,266-2,004,347 , GRCh37.p13 chr10: 47,423,171-47,423,252 ANXA8
    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
    nsv5907910copy number variation1nstd209human GRCh38 chr10: 47,657,059-47,660,309 , GRCh37.p13 chr10: 47,347,079-47,350,329 , GRCh37.p13 chr10|NW_003871068.1: 1,928,174-1,931,424 ANXA8
    nsv5867503copy number variation3nstd209human GRCh37.p13 chr10|NW_003871068.1: 1,828,469-1,837,491 , GRCh38 chr10: 47,557,354-47,566,376 DUSP8P1, GLUD1P6, 1 more genes
    nsv5866919copy number variation3nstd209human GRCh38 chr10: 47,940,778-47,943,080 , GRCh37.p13 chr10|NW_003871068.1: 2,130,674-2,132,976 ANXA8
    nsv5866477copy number variation3nstd209human GRCh37.p13 chr10|NW_003871068.1: 1,963,931-1,967,508 , GRCh38 chr10: 47,692,816-47,696,393 , GRCh37.p13 chr10: 47,382,836-47,386,413 SHLD2P3, RN7SL453P, 1 more genes
    nsv5860181copy number variation3nstd209human GRCh37.p13 chr10|NW_003871068.1: 1,963,930-1,974,443 , GRCh38 chr10: 47,692,815-47,703,328 , GRCh37.p13 chr10: 47,382,835-47,393,348 SHLD2P3, RN7SL453P, 1 more genes
    nsv5859968copy number variation3nstd209human GRCh38 chr10: 47,463,118-47,466,913 , GRCh37.p13 chr10|NW_003871068.1: 1,734,233-1,738,028 ANXA8
    nsv5857978copy number variation3nstd209human GRCh38 chr10: 47,683,244-47,689,336 , GRCh37.p13 chr10|NW_003871068.1: 1,954,359-1,960,451 , GRCh37.p13 chr10: 47,373,264-47,379,356 ANXA8, SHLD2P3
    nsv5857836copy number variation2nstd209human GRCh38 chr10: 47,585,649-47,591,609 , GRCh37.p13 chr10|NW_003871068.1: 1,856,764-1,862,724 LINC02675, ANXA8
    nsv5857241copy number variation3nstd209human GRCh37.p13 chr10|NW_003871068.1: 1,822,269-1,824,158 , GRCh38 chr10: 47,551,154-47,553,043 BMS1P2, ANXA8, 1 more genes
    nsv5856849copy number variation3nstd209human GRCh38 chr10: 47,966,979-47,971,311 , GRCh37.p13 chr10|NW_003871068.1: 2,156,875-2,161,207 ANXA8
    nsv5855281copy number variation3nstd209human GRCh38 chr10: 47,593,334-47,597,677 , GRCh37.p13 chr10|NW_003871068.1: 1,864,449-1,868,792 LINC02675, ANXA8
    nsv5852271copy number variation4nstd209human GRCh38 chr10: 47,664,648-47,676,686 , GRCh37.p13 chr10|NW_003871068.1: 1,935,763-1,947,801 , GRCh37.p13 chr10: 47,354,668-47,366,706 ANXA8
    nsv5851962copy number variation3nstd209human GRCh38 chr10: 47,620,581-47,623,432 , GRCh37.p13 chr10|NW_003871068.1: 1,891,696-1,894,547 ANXA8
    nsv5851727copy number variation3nstd209human GRCh38 chr10: 47,939,079-47,943,080 , GRCh37.p13 chr10|NW_003871068.1: 2,128,975-2,132,976 ANXA8
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