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Items: 1 to 20 of 464

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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
    nsv7094487copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,850,747-105,956,197 , GRCh38.p12 chr14: 105,384,410-105,489,860 TEX22, MTA1-DT, 5 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
    nsv7070878inversion1nstd229human GRCh38 chr14: 105,486,407-105,488,857 , GRCh37.p13 chr14|NW_004166863.1: 149,574-152,024 , GRCh37.p13 chr14: 105,952,744-105,955,194 CRIP1, TEDC1
    nsv6974490copy number variation1nstd229human GRCh38 chr14: 105,484,963-105,488,744 , GRCh37.p13 chr14|NW_004166863.1: 148,130-151,911 , GRCh37.p13 chr14: 105,951,300-105,955,081 TEDC1, CRIP1
    nsv6965650copy number variation1nstd229human GRCh38 chr14: 105,473,790-105,514,034 , GRCh37.p13 chr14: 105,940,127-105,980,371 , GRCh37.p13 chr14|NW_004166863.1: 136,957-177,201 CRIP1, TEDC1, 1 more genes
    nsv6964367copy number variation1nstd229human GRCh38 chr14: 105,488,428-105,498,454 , GRCh37.p13 chr14: 105,954,765-105,964,791 , GRCh37.p13 chr14|NW_004166863.1: 151,595-161,621 TEDC1, CRIP1
    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
    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
    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
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314048copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229 IGHD4-23, XRCC3, 329 more genes
    nsv6291499copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042 CDC42BPB, COA8, 133 more genes
    nsv6132861copy number variation1nstd213human GRCh37 chr14: 104,890,000-106,040,001 , GRCh38.p12 chr14: 104,423,663-105,573,664 AKT1, CRIP1, 40 more genes
    nsv6132582copy number variation1nstd213human GRCh37 chr14: 104,040,000-106,020,001 , GRCh38.p12 chr14: 103,573,663-105,533,002 PPP1R13B, GPR132, 57 more genes
    nsv5939683copy number variation1nstd209human GRCh38 chr14: 105,486,074-105,487,266 , GRCh37.p13 chr14|NW_004166863.1: 149,241-150,433 , GRCh37.p13 chr14: 105,952,411-105,953,603 CRIP1
    nsv5560907inversion1nstd206human GRCh37.p13 chr14|NW_004166863.1: 150,644-151,492 , GRCh38 chr14: 105,487,477-105,488,325 , GRCh37.p13 chr14: 105,953,814-105,954,662 CRIP1, TEDC1
    nsv5555887sequence alteration1nstd206human GRCh37.p13 chr14|NW_004166863.1: 150,648-151,546 , GRCh38 chr14: 105,487,481-105,488,379 , GRCh37.p13 chr14: 105,953,818-105,954,716 CRIP1, TEDC1
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