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Items: 1 to 20 of 1503

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112828copy number variation1nstd186human GRCh37 chr14: 106,071,380-106,178,036 , GRCh38.p12 chr14|NT_187600.1: 72,812-179,468 , GRCh38.p12 chr14: 105,605,043-105,711,699 , ELK2AP, 9 more genes
    nsv5979990inversion1nstd209human GRCh38 chr14: 105,626,484-105,858,518 , GRCh37.p13 chr14: 106,092,821-106,320,043 , ELK2AP, 19 more genes
    nsv5977780inversion1nstd209human GRCh38 chr14: 105,708,457-105,710,415 , GRCh37.p13 chr14: 106,174,794-106,176,752 IGH, IGHA1
    nsv5973552inversion1nstd209human GRCh38 chr14: 105,656,567-105,771,636 , GRCh37.p13 chr14: 106,122,904-106,237,973 , ELK2AP, 9 more genes
    nsv5973168inversion1nstd209human GRCh38 chr14: 105,589,366-105,862,476 , GRCh37.p13 chr14: 106,071,380-106,320,043 , ELK2AP, 25 more genes
    nsv5968136inversion1nstd209human GRCh38 chr14: 105,602,975-105,747,124 , GRCh37.p13 chr14: 106,071,380-106,213,461 , ELK2AP, 11 more genes
    nsv5947158copy number variation1nstd209human GRCh38 chr14: 105,646,452-105,711,448 , GRCh37.p13 chr14: 106,112,789-106,177,785 , ELK2AP, 4 more genes
    nsv5946235copy number variation1nstd209human GRCh38 chr14: 105,614,628-105,729,825 , GRCh37.p13 chr14: 106,080,965-106,196,162 , IGHGP, 10 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
    nsv5945930copy number variation1nstd209human GRCh38 chr14: 105,646,264-105,860,285 , GRCh37.p13 chr14: 106,112,601-106,320,043 , MIR4539, 16 more genes
    nsv5945884copy number variation1nstd209human GRCh38 chr14: 105,597,043-105,718,663 , GRCh37.p13 chr14: 106,071,380-106,185,000 , IGHE, 9 more genes
    nsv5945706copy number variation1nstd209human GRCh38 chr14: 105,589,424-105,861,306 , GRCh37.p13 chr14: 106,071,380-106,320,043 , MIR4538, 22 more genes
    nsv5945466copy number variation1nstd209human GRCh38 chr14: 105,708,802-105,711,868 , GRCh37.p13 chr14: 106,175,139-106,178,205 IGHA1, IGH
    nsv5944722copy number variation1nstd209human GRCh38 chr14: 105,647,328-105,710,739 , GRCh37.p13 chr14: 106,113,665-106,177,076 , ELK2AP, 4 more genes
    nsv5944684copy number variation1nstd209human GRCh38 chr14: 105,661,508-105,734,588 , GRCh37.p13 chr14: 106,127,845-106,200,925 , ELK2AP, 6 more genes
    nsv5943809copy number variation1nstd209human GRCh38 chr14: 105,588,595-105,708,743 , GRCh37.p13 chr14: 106,071,380-106,175,080 , IGHGP, 10 more genes
    nsv5943694copy number variation1nstd209human GRCh38 chr14: 105,647,993-105,709,926 , GRCh37.p13 chr14: 106,114,330-106,176,263 , ELK2AP, 4 more genes
    nsv5943441copy number variation1nstd209human GRCh38 chr14: 105,596,949-105,717,838 , GRCh37.p13 chr14: 106,071,380-106,184,175 , IGHGP, 9 more genes
    nsv5942873copy number variation1nstd209human GRCh38 chr14: 105,589,540-105,711,764 , GRCh37.p13 chr14: 106,071,380-106,178,101 , IGHGP, 9 more genes
    nsv5942416copy number variation1nstd209human GRCh38 chr14: 105,601,538-105,860,374 , GRCh37.p13 chr14: 106,071,380-106,320,043 , IGHG2, 21 more genes
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