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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5876678copy number variation1nstd209human GRCh38 chr2: 95,981,467-97,579,646 , GRCh37.p13 chr2: 96,647,215-98,196,109 , ARID5A, 48 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5381491copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,755,045-98,021,592 , GRCh38.p12 chr2: 96,089,297-97,285,797 LOC100421288, STARD7, 34 more genes
    nsv5381324copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 IGKV2OR2-8, LOC100506076, 42 more genes
    nsv5215020copy number variation1nstd204human GRCh38.p13 chr2: 96,060,101-97,188,600 , GRCh37.p13 chr2: 96,725,849-97,854,337 RN7SL313P, NCAPH, 33 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4738830copy number variation1nstd199human GRCh37 chr2: 96,734,555-98,241,090 , GRCh38.p12 chr2: 96,068,807-97,624,627 RN7SL313P, STARD7, 43 more genes
    nsv4728540copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,421,161-97,765,561 , GRCh38.p12 chr2: 95,755,413-97,099,824 DUSP2, RN7SL210P, 39 more genes
    nsv4728386copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,515,883-98,162,176 , GRCh38.p12 chr2: 95,850,135-97,545,713 LOC105373494, ARID5A, 47 more genes
    nsv4728289copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,544,602-97,706,860 , GRCh38.p12 chr2: 95,878,854-97,041,123 SNRNP200, FER1L5, 33 more genes
    nsv4684224copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 LOC100420569, CNNM3-DT, 42 more genes
    nsv4684160copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 96,737,083-98,261,802 , GRCh38.p12 chr2: 96,071,335-97,645,339 ADRA2B, COX5B, 45 more genes
    nsv4683954copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,780,545-96,994,037 , GRCh38.p12 chr2: 96,114,797-96,328,299 STARD7, ITPRIPL1, 8 more genes
    nsv4674518copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,939,073-97,086,456 , GRCh38.p12 chr2: 96,273,335-96,420,719 NCAPH, CIAO1, 2 more genes
    nsv4674453copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 96,712,139-98,254,657 , GRCh38.p12 chr2: 96,046,391-97,638,194 ADRA2B, DUSP2, 45 more genes
    nsv4674242copy number variation1nstd102humanUncertain significance GRCh37 chr2: 96,732,519-98,118,115 , GRCh38.p12 chr2: 96,066,771-97,501,652 DUSP2, ANKRD36, 42 more genes
    nsv4595873copy number variation1nstd183human GRCh37 chr2: 96,265,411-98,206,080 , GRCh38.p12 chr2: 95,599,663-97,589,617 , CIAO1, 57 more genes
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