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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047201inversion1nstd229human GRCh38 chr2: 113,135,467-114,194,806 , GRCh37.p13 chr2: 113,893,044-114,952,383 SLC35F5, ACRP1, 26 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv7042586inversion1nstd229human GRCh38 chr2: 111,572,275-118,829,502 , GRCh37.p13 chr2: 112,329,852-119,587,078 LOC105373579, NT5DC4, 103 more genes
    nsv6696166copy number variation1nstd229human GRCh38 chr2: 113,165,730-113,169,455 , GRCh37.p13 chr2: 113,923,307-113,927,032 PSD4
    nsv6684166copy number variation1nstd229human GRCh38 chr2: 113,176,068-113,185,861 , GRCh37.p13 chr2: 113,933,645-113,943,438 PSD4
    nsv6682767copy number variation1nstd229human GRCh38 chr2: 113,186,901-113,193,200 , GRCh37.p13 chr2: 113,944,478-113,950,777 PSD4
    nsv6679384copy number variation1nstd229human GRCh38 chr2: 113,064,901-113,421,800 , GRCh37.p13 chr2: 113,822,478-114,179,377 LOC107985936, PAX8-AS1, 8 more genes
    nsv6678375copy number variation1nstd229human GRCh38 chr2: 113,153,659-113,157,034 , GRCh37.p13 chr2: 113,911,236-113,914,611 PSD4
    nsv6547752inversion1nstd223human GRCh38 chr2: 113,149,082-113,162,526 , GRCh37.p13 chr2: 113,906,659-113,920,103 PSD4
    nsv6545977inversion1nstd223human GRCh38 chr2: 113,161,446-113,162,133 , GRCh37.p13 chr2: 113,919,023-113,919,710 PSD4
    nsv6349890copy number variation1nstd223human GRCh38 chr2: 113,177,553-113,178,893 , GRCh37.p13 chr2: 113,935,130-113,936,470 PSD4
    nsv6337104copy number variation1nstd223human GRCh38 chr2: 113,064,901-113,421,800 , GRCh37.p13 chr2: 113,822,478-114,179,377 LINC02966, IL1RN, 8 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314748copy number variation1nstd102humanPathogenic GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432 MED15P9, TMEM37, 474 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313770copy number variation1nstd102humanPathogenic GRCh37 chr2: 113,188,197-128,144,700 , GRCh38.p12 chr2: 112,430,620-127,387,124 LOC105373575, RPS20P11, 174 more genes
    nsv6291353copy number variation1nstd102humanPathogenic GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036 LINC01120, LOC105373585, 490 more genes
    nsv6291237copy number variation1nstd102humanUncertain significance GRCh37 chr2: 113,295,194-114,085,649 , GRCh38.p12 chr2: 112,537,617-113,328,072 CKAP2L, LOC105373567, 30 more genes
    nsv6291014copy number variation1nstd102humanUncertain significance GRCh37 chr2: 113,609,489-115,817,535 , GRCh38.p12 chr2: 112,851,912-115,059,958 PSD4, PGM5P4, 43 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
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