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Items: 1 to 20 of 111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5442341copy number variation1nstd206human GRCh38 chr2: 101,144,069-101,150,109 , GRCh37.p13 chr2: 101,760,531-101,766,571 TBC1D8-AS1, TBC1D8
    nsv5281322copy number variation1nstd204human GRCh38.p13 chr2: 100,864,060-101,514,976 , GRCh37.p13 chr2: 101,480,522-102,131,438 LINC01870, LOC105373511, 17 more genes
    nsv5217676copy number variation1nstd204human GRCh38.p13 chr2: 100,959,101-101,514,900 , GRCh37.p13 chr2: 101,575,563-102,131,362 RNF149, NPAS2, 17 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894856copy number variation1nstd200human GRCh38 chr2: 100,864,090-101,514,954 , GRCh37.p13 chr2: 101,480,552-102,131,416 CREG2, LOC105373510, 17 more genes
    nsv4781672copy number variation1nstd200human GRCh37 chr2: 101,480,552-102,131,416 , GRCh38.p12 chr2: 100,864,090-101,514,954 LOC105373512, BBIP1P1, 17 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
    nsv4558802mobile element insertion1nstd166human GRCh37.p13 chr2: 101,769,666-101,769,666 , GRCh38.p12 chr2: 101,153,204-101,153,204 TBC1D8-AS1, TBC1D8
    nsv4312591inversion1nstd166human GRCh37.p13 chr2: 97,201,014-102,197,203 , GRCh38.p12 chr2: 96,535,277-101,580,741 , CNGA3, 106 more genes
    nsv4056061copy number variation1nstd166human GRCh37.p13 chr2: 101,473,704-101,841,526 , GRCh38.p12 chr2: 100,857,242-101,225,064 NPAS2, RPL31, 6 more genes
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 DAZAP2P1, RPL36AP16, 2991 more genes
    nsv3907419copy number variation1nstd102humanUncertain significance NCBI36 chr2: 100,688,511-101,449,625 , GRCh37 chr2: 101,322,079-102,083,193 , GRCh38 chr2: 100,705,617-101,466,731 LOC100420429, MIR5696, 17 more genes
    nsv3907326copy number variation1nstd102humanPathogenic GRCh38 chr2: 97,672,522-110,211,318 , GRCh37 chr2: 98,288,985-110,968,895 , NCBI36 chr2: 97,655,417-110,326,184 RPL22P11, PANTR1, 212 more genes
    nsv3906654copy number variation1nstd102humanPathogenic GRCh38 chr2: 91,443,218-102,334,856 , NCBI36 chr2: 90,981,410-102,317,748 , GRCh37 chr2: 91,617,683-102,951,316 CHEK2P3, LMAN2L, 197 more genes
    nsv3906499copy number variation1nstd102humanPathogenic NCBI36 chr2: 100,361,404-108,455,759 , GRCh37 chr2: 100,994,972-109,089,327 , GRCh38 chr2: 100,378,510-108,472,871 LOC105373511, ANAPC1P6, 132 more genes
    nsv3904828copy number variation1nstd102humanUncertain significance GRCh38 chr2: 101,080,018-101,646,523 , NCBI36 chr2: 101,062,912-101,629,417 , GRCh37 chr2: 101,696,480-102,262,985 RNF149, LINC01870, 13 more genes
    nsv3902899copy number variation1nstd102humanPathogenic NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986 MTCO3P45, RPS21P2, 325 more genes
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