U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 977

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148227copy number variation1nstd102humanPathogenic GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138 TNFAIP2, IGHV4-30-2, 306 more genes
    nsv7137201copy number variation1nstd102humanPathogenic GRCh37 chr14: 103,636,647-107,285,437 , GRCh38.p12 chr14: 103,170,310-106,877,229 IGHD, IGH, 281 more genes
    nsv7071453inversion1nstd229human GRCh38 chr14: 104,922,043-106,758,290 , GRCh37.p13 chr14: 105,388,380-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 1-1,421,457 IGHD1-14, IGHVII-53-1, 206 more genes
    nsv7071102inversion1nstd229human GRCh38 chr14: 106,082,027-106,821,246 , GRCh37.p13 chr14|NW_004166863.1: 1,008,127-1,484,413 GOLGA4P2, IGHV3-71, 117 more genes
    nsv7068661inversion1nstd229human GRCh38 chr14: 105,907,228-106,196,706 , GRCh37.p13 chr14|NW_004166863.1: 570,395-859,873 IGHV3-15, IGHV1-12, 39 more genes
    nsv7064373inversion1nstd229human GRCh38 chr14: 106,092,726-106,119,335 , GRCh37.p13 chr14|NW_004166863.1: 755,893-782,502 IGHV5-10-1, IGHV3-11, 2 more genes
    nsv6975135copy number variation1nstd229human GRCh38 chr14: 106,075,201-106,367,300 , GRCh37.p13 chr14|NW_004166863.1: 738,368-1,008,126 IGHV3-23, IGHV1-18, 46 more genes
    nsv6974867copy number variation1nstd229human GRCh38 chr14: 106,104,001-106,325,400 , GRCh37.p13 chr14|NW_004166863.1: 767,168-988,567 IGHV1-12, IGHVIII-25-1, 32 more genes
    nsv6972478copy number variation1nstd229human GRCh38 chr14: 105,863,240-106,622,360 , GRCh37.p13 chr14|NW_004166863.1: 526,407-1,285,527 IGHVII-15-1, IGHVIII-5-2, 137 more genes
    nsv6972090copy number variation1nstd229human GRCh38 chr14: 105,863,258-106,373,701 , GRCh37.p13 chr14|NW_004166863.1: 526,425-1,008,126 IGHD4-11, IGHD5-5, 99 more genes
    nsv6969767copy number variation1nstd229human GRCh38 chr14: 106,114,611-106,121,094 , GRCh37.p13 chr14|NW_004166863.1: 777,778-784,261 IGHV1-12, IGHVIII-11-1, 2 more genes
    nsv6969658copy number variation1nstd229human GRCh38 chr14: 105,863,215-106,421,772 , GRCh37.p13 chr14|NW_004166863.1: 526,382-1,008,126 IGHD3-22, IGHD4-17, 106 more genes
    nsv6969329copy number variation1nstd229human GRCh38 chr14: 105,973,328-106,246,630 , GRCh37.p13 chr14|NW_004166863.1: 636,495-909,797 IGHVII-20-1, IGHV3-64D, 31 more genes
    nsv6969166copy number variation1nstd229human GRCh38 chr14: 105,543,903-106,485,920 , GRCh37.p13 chr14: 106,010,240-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 236,423-1,025,122 MIR8071-1, IGHVII-15-1, 137 more genes
    nsv6967675copy number variation1nstd229human GRCh38 chr14: 105,863,257-106,622,360 , GRCh37.p13 chr14|NW_004166863.1: 526,424-1,285,527 IGHV3-54, IGHV3-50, 137 more genes
    nsv6966723copy number variation1nstd229human GRCh38 chr14: 105,863,250-106,421,707 , GRCh37.p13 chr14|NW_004166863.1: 526,417-1,008,126 IGHD2-2, IGHD2-21, 106 more genes
    nsv6964656copy number variation1nstd229human GRCh38 chr14: 105,864,638-106,184,903 , GRCh37.p13 chr14|NW_004166863.1: 527,805-848,070 IGHVIII-5-1, IGHJ1, 63 more genes
    nsv6963766copy number variation1nstd229human GRCh38 chr14: 105,863,211-106,373,744 , GRCh37.p13 chr14|NW_004166863.1: 526,378-1,008,126 IGHD5-24, IGHV7-27, 99 more genes
    nsv6962829copy number variation1nstd229human GRCh38 chr14: 105,891,720-106,810,442 , GRCh37.p13 chr14|NW_004166863.1: 1,008,127-1,473,609 IGHVII-49-1, IGHV1-14, 151 more genes
    nsv6962425copy number variation1nstd229human GRCh38 chr14: 105,863,194-106,622,360 , GRCh37.p13 chr14|NW_004166863.1: 526,361-1,285,527 IGHV3-30-2, IGHVIII-11-1, 137 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center