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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5868064copy number variation1nstd209human GRCh38 chr2: 94,690,991-95,007,035 , GRCh37.p13 chr2: 95,356,717-95,618,108 , GRCh37.p13 chr2|NW_003571032.1: 128,567-389,939 RPS24P6, SNX18P14, 14 more genes
    nsv5568046copy number variation1nstd207human GRCh38 chr2: 94,753,519-94,753,828 , GRCh37.p13 chr2: 95,419,264-95,419,573 , GRCh37.p13 chr2|NW_003571032.1: 191,095-191,404 FAM95A
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4908083copy number variation1nstd200human GRCh38 chr2: 94,757,008-94,757,143 , GRCh37.p13 chr2|NW_003571032.1: 194,584-194,719 , GRCh37.p13 chr2: 95,422,753-95,422,888 FAM95A
    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
    nsv4713039copy number variation1nstd195human GRCh37 chr2: 95,419,249-95,419,250 , GRCh38.p12 chr2: 94,753,504-94,753,505 FAM95A
    nsv4586772copy number variation1nstd183human GRCh37 chr2: 95,421,441-95,457,786 , GRCh38.p12 chr2: 94,755,696-94,792,041 SNX18P14, FAM95A, 2 more genes
    nsv4519091copy number variation1nstd166human GRCh37.p13 chr2: 95,326,170-95,629,000 , GRCh38.p12 chr2: 94,660,448-94,963,255 CNN2P8, LOC442028, 13 more genes
    nsv4406843copy number variation1nstd174human GRCh37 chr2: 95,326,217-95,433,630 , GRCh38.p12 chr2: 94,660,492-94,767,885 FAM95A, CNN2P8, 5 more genes
    nsv4400291copy number variation1nstd174human GRCh37 chr2: 95,421,441-95,457,786 , GRCh38.p12 chr2: 94,755,696-94,792,041 CYP4F32P, FAM95A, 2 more genes
    nsv4399594copy number variation1nstd174human GRCh37 chr2: 95,418,907-95,564,702 , GRCh38.p12 chr2: 94,753,162-94,898,957 FAM95A, TEKT4, 6 more genes
    nsv4070680copy number variation1nstd166human GRCh37.p13 chr2: 95,425,600-95,433,400 , GRCh38.p12 chr2: 94,759,855-94,767,655 FAM95A, CYP4F32P, 1 more genes
    nsv3914520copy number variation1nstd102humanUncertain significance NCBI36 chr2: 91,624,387-95,105,188 , GRCh37.p13 chr2: 92,260,660-95,741,461 , GRCh38.p12 chr2: 92,072,634-95,075,716 GXYLT1P7, AQP7B, 21 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
    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
    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
    nsv3896048copy number variation1nstd102humanLikely benign NCBI36 chr2: 94,780,662-95,704,515 , GRCh38 chr2: 94,751,190-95,675,040 , GRCh37 chr2: 95,618,109-96,340,788 LOC100421292, LOC105373488, 38 more genes
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