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Items: 1 to 20 of 975

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    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
    nsv7069810inversion1nstd229human GRCh38 chr14: 106,330,249-106,821,247 , GRCh37.p13 chr14|NW_004166863.1: 1,008,127-1,484,414 IGHVII-46-1, LINC00221, 82 more genes
    nsv7069132inversion1nstd229human GRCh38 chr14: 106,304,597-106,628,256 , GRCh37.p13 chr14|NW_004166863.1: 967,764-1,291,423 IGHVII-44-2, IGHVII-28-1, 56 more genes
    nsv7059425inversion1nstd229human GRCh38 chr14: 106,596,791-106,638,801 , GRCh37.p13 chr14|NW_004166863.1: 1,259,958-1,301,968 IGHV4-55, IGHV3-54, 10 more genes
    nsv6977741copy number variation1nstd229human GRCh38 chr14: 106,619,519-106,631,869 , GRCh37.p13 chr14|NW_004166863.1: 1,282,686-1,295,036 IGHV4-59, IGHV1-58, 3 more genes
    nsv6975991copy number variation1nstd229human GRCh38 chr14: 106,604,001-106,618,200 , GRCh37.p13 chr14|NW_004166863.1: 1,267,168-1,281,367 IGHV3-57, IGHV4-55, 2 more genes
    nsv6975157copy number variation1nstd229human GRCh38 chr14: 106,611,642-106,658,130 , GRCh37.p13 chr14|NW_004166863.1: 1,274,809-1,321,297 IGHVII-62-1, IGHV3-60, 12 more genes
    nsv6974097copy number variation1nstd229human GRCh38 chr14: 106,576,304-106,657,697 , GRCh37.p13 chr14|NW_004166863.1: 1,239,471-1,320,864 LOC102724977, IGHV4-55, 21 more genes
    nsv6972800copy number variation1nstd229human GRCh38 chr14: 106,615,774-106,624,436 , GRCh37.p13 chr14|NW_004166863.1: 1,278,941-1,287,603 IGHV3-57, IGH, 1 more genes
    nsv6972720copy number variation1nstd229human GRCh38 chr14: 106,427,152-106,786,879 , GRCh37.p13 chr14|NW_004166863.1: 1,136,601-1,405,282 IGHV3-62, IGHV4-55, 57 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
    nsv6971739copy number variation1nstd229human GRCh38 chr14: 106,615,801-106,619,600 , GRCh37.p13 chr14|NW_004166863.1: 1,278,968-1,282,767 IGH, IGHV3-57
    nsv6968664copy number variation1nstd229human GRCh38 chr14: 106,611,085-106,617,528 , GRCh37.p13 chr14|NW_004166863.1: 1,274,252-1,280,695 IGHV3-57, IGH
    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
    nsv6966914copy number variation1nstd229human GRCh38 chr14: 106,604,889-106,623,333 , GRCh37.p13 chr14|NW_004166863.1: 1,268,056-1,286,500 IGHV7-56, IGH, 3 more genes
    nsv6966032copy number variation1nstd229human GRCh38 chr14: 106,167,021-106,622,879 , GRCh37.p13 chr14|NW_004166863.1: 830,188-1,286,046 IGHVIII-16-1, IGHV3-33-2, 74 more genes
    nsv6965280copy number variation1nstd229human GRCh38 chr14: 106,616,324-106,625,997 , GRCh37.p13 chr14|NW_004166863.1: 1,279,491-1,289,164 IGHV4-59, IGHV3-57, 2 more genes
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