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 3014

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971496insertion1nstd209human GRCh37.p13 chr14|NW_004166863.1: 931,256-931,256 , GRCh38 chr14: 106,268,089-106,268,089 IGH, IGHV3-23
    nsv5947248copy number variation1nstd209human GRCh38 chr14: 106,000,462-106,417,808 , GRCh37.p13 chr14|NW_004166863.1: 663,629-1,008,126 IGHV3-37, IGHV3-6, 63 more genes
    nsv5947220copy number variation1nstd209human GRCh38 chr14: 106,266,875-106,267,241 , GRCh37.p13 chr14|NW_004166863.1: 930,042-930,408 IGHV3-23, IGH
    nsv5947112copy number variation1nstd209human GRCh38 chr14: 105,865,458-106,373,660 , GRCh37.p13 chr14|NW_004166863.1: 528,625-1,008,126 IGHD4-11, IGHV3-30-2, 93 more genes
    nsv5946948copy number variation1nstd209human GRCh38 chr14: 105,863,325-106,373,615 , GRCh37.p13 chr14|NW_004166863.1: 526,492-1,008,126 IGHVII-30-21, IGHD5-24, 99 more genes
    nsv5946828copy number variation1nstd209human GRCh38 chr14: 105,864,629-106,737,110 , GRCh37.p13 chr14|NW_004166863.1: 527,796-1,400,277 , IGHVII-26-2, 160 more genes
    nsv5946696copy number variation1nstd209human GRCh38 chr14: 105,891,201-106,586,373 , GRCh37.p13 chr14|NW_004166863.1: 554,368-1,249,540 , IGHV1-45, 115 more genes
    nsv5946227copy number variation1nstd209human GRCh38 chr14: 105,863,257-106,276,550 , GRCh37.p13 chr14|NW_004166863.1: 526,424-939,717 IGHD5-18, IGHV3-16, 76 more genes
    nsv5946084copy number variation1nstd209human GRCh38 chr14: 105,864,636-106,359,789 , GRCh37.p13 chr14|NW_004166863.1: 527,803-1,008,126 IGHVIII-22-2, IGHVII-28-1, 93 more genes
    nsv5946083copy number variation1nstd209human GRCh38 chr14: 105,691,298-106,606,057 , GRCh37.p13 chr14: 106,157,635-106,929,356 , GRCh37.p13 chr14|NW_004166863.1: 516,901-1,269,224 , IGHV3-41, 148 more genes
    nsv5945938copy number variation1nstd209human GRCh38 chr14: 105,916,842-106,775,157 , GRCh37.p13 chr14|NW_004166863.1: 1,008,127-1,438,324 , IGHV3-41, 132 more genes
    nsv5945285copy number variation1nstd209human GRCh38 chr14: 105,863,965-106,775,248 , GRCh37.p13 chr14|NW_004166863.1: 527,132-1,405,282 , IGHVII-65-1, 165 more genes
    nsv5945225copy number variation1nstd209human GRCh38 chr14: 106,185,769-106,875,402 , GRCh37.p13 chr14: 106,817,885-107,283,610 , GRCh37.p13 chr14|NW_004166863.1: 1,008,127-1,523,386 , LINC00226, 113 more genes
    nsv5944737copy number variation1nstd209human GRCh38 chr14: 105,863,395-106,556,923 , GRCh37.p13 chr14|NW_004166863.1: 526,562-1,220,090 , IGHVII-40-1, 125 more genes
    nsv5944305copy number variation1nstd209human GRCh38 chr14: 105,901,160-106,373,658 , GRCh37.p13 chr14|NW_004166863.1: 564,327-1,008,126 IGHV3-15, IGHV1-12, 76 more genes
    nsv5944219copy number variation1nstd209human GRCh38 chr14: 105,864,360-106,790,755 , GRCh37.p13 chr14|NW_004166863.1: 527,527-1,405,282 , IGHV3-65, 165 more genes
    nsv5944042copy number variation1nstd209human GRCh38 chr14: 105,863,858-106,578,742 , GRCh37.p13 chr14|NW_004166863.1: 527,025-1,241,909 , IGHV3-19, 127 more genes
    nsv5944033copy number variation1nstd209human GRCh38 chr14: 105,864,311-106,586,390 , GRCh37.p13 chr14|NW_004166863.1: 527,478-1,249,557 , IGHJ2, 129 more genes
    nsv5943749copy number variation1nstd209human GRCh38 chr14: 105,863,861-106,276,544 , GRCh37.p13 chr14|NW_004166863.1: 527,028-939,711 IGHD2-2, IGHJ1P, 75 more genes
    nsv5943478copy number variation1nstd209human GRCh38 chr14: 105,863,859-106,301,390 , GRCh37.p13 chr14|NW_004166863.1: 527,026-964,557 IGHD5-18, IGHD4-23, 80 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center