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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3909861copy number variation1nstd102humanUncertain significance NCBI36 chr2: 95,250,584-95,437,797 , GRCh37.p13 chr2: 95,886,857-96,074,070 , GRCh38.p12 chr2: 95,221,109-95,408,322 PROM2, FAHD2A, 2 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 PROM2, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 PROM2, CYP1B1-AS1, 1649 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 PROM2, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 PROM2, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 PROM2, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 PROM2, MTND2P22, 3724 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 PROM2, MTCO3P45, 325 more genes
    nsv3877583copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,529,039-108,518,266 , GRCh38.p12 chr2: 94,863,294-107,901,810 PROM2, RPL27AP4, 242 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 PROM2, CHEK2P3, 197 more genes
    nsv3899291copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,618,109-103,868,854 , GRCh38 chr2: 94,817,406-103,252,396 , NCBI36 chr2: 94,846,878-103,235,286 PROM2, IGKV2OR2-10, 178 more genes
    nsv3889077copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,691,600-100,587,394 , GRCh38.p12 chr2: 95,025,855-99,970,932 PROM2, TMEM127, 114 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 PROM2, ACTG2, 1713 more genes
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 PROM2, ADRA2B, 130 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 PROM2, LOC100421292, 38 more genes
    nsv4453674copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,800,306-96,097,247 , GRCh38.p12 chr2: 95,134,561-95,431,499 PROM2, ZNF2, 7 more genes
    nsv3892769copy number variation1nstd102humanUncertain significance NCBI36 chr2: 95,173,125-95,460,974 , GRCh37 chr2: 95,809,398-96,097,247 , GRCh38 chr2: 95,143,653-95,431,499 PROM2, ZNF2, 7 more genes
    nsv6313735copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,341,387-96,735,978 , GRCh38.p12 chr2: 94,675,662-96,070,230 PROM2, TRIM43, 48 more genes
    nsv3872310copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,341,387-96,719,347 , GRCh38.p12 chr2: 94,675,662-96,053,599 PROM2, GPAT2P1, 48 more genes
    nsv3904893copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,799,814-96,159,275 , GRCh38 chr2: 95,134,069-95,493,527 , NCBI36 chr2: 95,163,541-95,523,002 PROM2, ZNF2, 10 more genes
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