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 314

    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
    nsv6975434copy number variation1nstd229human GRCh38 chr14: 106,821,363-106,828,377 , GRCh37.p13 chr14|NW_004166863.1: 1,484,530-1,491,544 IGHV3-76, IGHVII-74-1, 2 more genes
    nsv6974415copy number variation1nstd229human GRCh38 chr14: 106,669,849-106,822,025 , GRCh37.p13 chr14|NW_004166863.1: 1,405,283-1,485,192 IGHV3-72, IGHV3-75, 20 more genes
    nsv6970902copy number variation1nstd229human GRCh37.p13 chr14|NW_004166863.1: 1,482,275-1,513,070 , GRCh38 chr14: 106,819,108-106,849,903 IGHVII-74-1, MIR5195, 5 more genes
    nsv6970628copy number variation1nstd229human GRCh38 chr14: 106,806,075-106,860,976 , GRCh37.p13 chr14|NW_004166863.1: 1,469,242-1,523,386 MIR5195, IGH, 6 more genes
    nsv6964657copy number variation1nstd229human GRCh38 chr14: 106,766,747-106,850,905 , GRCh37.p13 chr14|NW_004166863.1: 1,429,914-1,514,072 IGH, IGHV3-72, 10 more genes
    nsv6961446copy number variation1nstd229human GRCh38 chr14: 106,819,813-106,829,634 , GRCh37.p13 chr14|NW_004166863.1: 1,482,980-1,492,801 IGHVII-74-1, IGHV3-76, 2 more genes
    nsv6961201copy number variation1nstd229human GRCh38 chr14: 106,806,297-106,856,907 , GRCh37.p13 chr14|NW_004166863.1: 1,469,464-1,520,074 IGHVIII-76-1, IGHV3-74, 6 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6635619copy number variation1nstd227human GRCh38.p12 chr14: 105,601,281-106,879,456 , GRCh37 chr14: 106,067,618-107,287,663 , GRCh38.p12 chr14|NT_187600.1: 72,812-1,214,078 ELK2AP, IGH, 198 more genes
    nsv6635373copy number variation1nstd227human GRCh38.p12 chr14: 105,573,256-106,879,456 , GRCh37 chr14: 106,016,434-107,287,663 , GRCh38.p12 chr14|NT_187600.1: 17,095-1,214,078 ELK2AP, IGH, 202 more genes
    nsv6622473copy number variation1nstd224human GRCh37 chr14: 107,211,012-107,281,980 , GRCh38.p12 chr14: 106,802,774-106,873,771 , GRCh38.p12 chr14|NT_187600.1: 1,293,948-1,351,393 IGH, IGHV7-81, 11 more genes
    nsv6622444copy number variation1nstd224human GRCh37 chr14: 107,229,408-107,250,080 , GRCh38.p12 chr14: 106,821,177-106,841,864 , GRCh38.p12 chr14|NT_187600.1: 1,312,351-1,333,038 IGHVIII-76-1, IGHV3-76, 3 more genes
    nsv6622443copy number variation1nstd224human GRCh37 chr14: 107,209,113-107,282,024 , GRCh38.p12 chr14: 106,800,875-106,873,815 , GRCh38.p12 chr14|NT_187600.1: 1,292,049-1,351,393 IGHVIII-76-1, IGHV5-78, 11 more genes
    nsv6622442copy number variation1nstd224human GRCh37 chr14: 107,193,676-107,263,150 , GRCh38.p12 chr14: 106,785,438-106,854,935 , GRCh38.p12 chr14|NT_187600.1: 1,276,612-1,346,109 IGHVII-74-1, IGHV3-74, 8 more genes
    nsv6622440copy number variation1nstd224human GRCh37 chr14: 106,651,388-107,283,150 , GRCh38.p12 chr14: 106,194,717-106,874,941 IGHVIII-67-3, IGHVIII-47-1, 111 more genes
    nsv6622439copy number variation1nstd224human GRCh37 chr14: 106,471,356-107,287,663 , GRCh38.p12 chr14: 106,005,207-106,879,456 , GRCh38.p12 chr14|NT_187600.1: 475,711-1,214,078 IGHVIII-82, IGHVIII-67-3, 136 more genes
    nsv6622438copy number variation1nstd224human GRCh37 chr14: 105,773,028-107,287,663 , GRCh38.p12 chr14: 105,306,691-106,879,456 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 CRIP2, BRF1, 214 more genes
    nsv6621999copy number variation1nstd224human GRCh37 chr14: 107,229,408-107,263,150 , GRCh38.p12 chr14: 106,821,177-106,854,935 IGH, IGHVIII-76-1, 5 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