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Items: 1 to 20 of 57

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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 NCAPH, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 NCAPH, CYP1B1-AS1, 1649 more genes
    nsv4452469copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,552,903-98,118,115 , GRCh38.p12 chr2: 95,887,155-97,501,652 NCAPH, CNNM4, 47 more genes
    nsv5381324copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 NCAPH, IGKV2OR2-8, 42 more genes
    nsv3900766copy number variation1nstd102humanPathogenic GRCh38 chr2: 96,073,560-97,513,144 , GRCh37 chr2: 96,739,308-98,066,294 , NCBI36 chr2: 96,103,035-97,496,039 NCAPH, CIAO1, 42 more genes
    nsv3902782copy number variation1nstd102humanPathogenic GRCh38 chr2: 95,879,602-97,285,797 , GRCh37 chr2: 96,545,350-98,013,866 , NCBI36 chr2: 95,909,077-97,380,005 NCAPH, SNRNP200, 39 more genes
    nsv5381491copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,755,045-98,021,592 , GRCh38.p12 chr2: 96,089,297-97,285,797 NCAPH, LOC100421288, 34 more genes
    nsv3903903copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,766,560-98,013,866 , GRCh38 chr2: 96,100,812-97,285,797 , NCBI36 chr2: 96,130,287-97,380,005 NCAPH, ANKRD36, 34 more genes
    nsv3899027copy number variation1nstd102humanPathogenic NCBI36 chr2: 96,103,035-97,092,174 , GRCh37 chr2: 96,739,308-97,728,447 , GRCh38 chr2: 96,073,560-97,062,710 NCAPH, LOC105373496, 29 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 NCAPH, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 NCAPH, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 NCAPH, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 NCAPH, MTND2P22, 3724 more genes
    nsv3876227copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886 NCAPH, RNU4-8P, 346 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 NCAPH, MTCO3P45, 325 more genes
    nsv3877583copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,529,039-108,518,266 , GRCh38.p12 chr2: 94,863,294-107,901,810 NCAPH, 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 NCAPH, 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 NCAPH, 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 NCAPH, TMEM127, 114 more genes
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