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Items: 1 to 20 of 2080

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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
    nsv7073468inversion1nstd229human GRCh38 chr14: 106,672,906-106,816,896 , GRCh37.p13 chr14|NW_004166863.1: 1,405,283-1,480,063 IGHV3-72, IGHVIII-67-3, 17 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
    nsv7070042inversion1nstd229human GRCh38 chr14: 106,645,662-106,783,676 , GRCh37.p13 chr14|NW_004166863.1: 1,308,829-1,405,282 IGHVIII-67-3, IGH, 21 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
    nsv7067046inversion1nstd229human GRCh38 chr14: 106,682,541-106,682,610 , GRCh37.p13 chr14|NW_004166863.1: 1,345,708-1,345,777 SLC20A1P1, IGH
    nsv7065021inversion1nstd229human GRCh38 chr14: 106,636,513-106,773,882 , GRCh37.p13 chr14|NW_004166863.1: 1,299,680-1,405,282 IGHVII-65-1, IGHV2-70D, 25 more genes
    nsv6977795copy number variation1nstd229human GRCh38 chr14: 106,669,507-106,681,377 , GRCh37.p13 chr14|NW_004166863.1: 1,332,674-1,344,544 SLC20A1P1, IGHV3-66, 3 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
    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
    nsv6964724copy number variation1nstd229human GRCh38 chr14: 106,610,741-106,684,592 , GRCh37.p13 chr14|NW_004166863.1: 1,273,908-1,347,759 IGHV3-65, LOC102724977, 18 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
    nsv6960440copy number variation1nstd229human GRCh38 chr14: 106,579,248-106,680,838 , GRCh37.p13 chr14|NW_004166863.1: 1,242,415-1,344,005 IGHV4-59, GOLGA4P3, 26 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
    nsv6635138copy number variation1nstd227human GRCh38.p12 chr14: 105,464,069-106,493,296 , GRCh37 chr14: 105,930,406-106,949,307 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 CRIP1, CRIP2, 190 more genes
    nsv6634944copy number variation1nstd227human GRCh38.p12 chr14: 105,450,460-106,683,566 , GRCh37 chr14: 105,916,797-107,139,583 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 CRIP1, CRIP2, 190 more genes
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