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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7039561inversion1nstd229human GRCh38 chr2: 112,945,161-113,099,965 , GRCh37.p13 chr2: 113,702,738-113,857,542 IL36G, POLR2DP1, 7 more genes
    nsv6692272copy number variation1nstd229human GRCh38 chr2: 113,057,962-113,070,374 , GRCh37.p13 chr2: 113,815,539-113,827,951 IL36RN, IL1F10
    nsv6690747copy number variation1nstd229human GRCh38 chr2: 112,960,556-113,135,779 , GRCh37.p13 chr2: 113,718,133-113,893,356 IL36G, POLR2DP1, 7 more genes
    nsv6680054copy number variation1nstd229human GRCh38 chr2: 113,061,404-113,061,633 , GRCh37.p13 chr2: 113,818,981-113,819,210 IL36RN
    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
    nsv6344150copy number variation1nstd223human GRCh38 chr2: 113,010,465-113,106,661 , GRCh37.p13 chr2: 113,768,042-113,864,238 IL1RN, IL36RN, 4 more genes
    nsv6343530copy number variation1nstd223human GRCh38 chr2: 112,960,556-113,135,775 , GRCh37.p13 chr2: 113,718,133-113,893,352 IL1RN, IL36RN, 7 more genes
    nsv6340993copy number variation1nstd223human GRCh38 chr2: 113,058,801-113,063,100 , GRCh37.p13 chr2: 113,816,378-113,820,677 IL36RN
    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
    nsv6311288copy number variation2nstd102humanPathogenic GRCh37 chr2: 113,817,016-113,890,448 , GRCh38.p12 chr2: 113,059,439-113,132,871 IL1F10, RNU6-1180P, 2 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
    nsv6290686copy number variation1nstd102humanUncertain significance GRCh38 chr2: 112,924,872-113,105,404 , GRCh37.p13 chr2: 113,682,449-113,862,981 IL36A, IL36G, 8 more genes
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