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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908534copy number variation1nstd102humanBenign GRCh37 chr19: 1,950,503-1,952,090 , GRCh38.p12 chr19: 1,950,504-1,952,091 CSNK1G2, CSNK1G2-AS1
    nsv3891154copy number variation1nstd102humanBenign GRCh37 chr19: 1,952,590-2,050,814 , GRCh38.p12 chr19: 1,952,591-2,050,815 CSNK1G2, MKNK2, 3 more genes
    nsv3903075copy number variation1nstd102humanBenign GRCh37 chr19: 1,937,178-1,961,474 , GRCh38.p12 chr19: 1,937,179-1,961,475 CSNK1G2, CSNK1G2-AS1, 1 more genes
    nsv3896917copy number variation1nstd102humanBenign GRCh37 chr19: 1,937,178-1,951,495 , GRCh38.p12 chr19: 1,937,179-1,951,496 CSNK1G2, CSNK1G2-AS1, 1 more genes
    nsv3893400copy number variation1nstd102humanBenign GRCh37 chr19: 1,937,178-1,951,332 , GRCh38.p12 chr19: 1,937,179-1,951,333 CSNK1G2, CSNK1G2-AS1, 1 more genes
    nsv3922397copy number variation1nstd102humanBenign GRCh38 chr19: 1,911,810-1,952,591 , NCBI36 chr19: 1,862,809-1,903,590 , GRCh37 chr19: 1,911,809-1,952,590 CSNK1G2, ADAT3, 3 more genes
    nsv3910710copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,549,143-4,288,717 , NCBI36 chr19: 1,500,143-4,239,717 , GRCh38 chr19: 1,549,144-4,288,720 CSNK1G2, EBI3, 110 more genes
    nsv3922151copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh38 chr19: 945,098-1,972,299 , GRCh37 chr19: 945,098-1,972,298 CSNK1G2, MIR1909, 58 more genes
    nsv3913614copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,678,561-2,257,495 , GRCh37 chr19: 1,727,561-2,306,495 , GRCh38 chr19: 1,727,562-2,306,496 CSNK1G2, JSRP1, 30 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 CSNK1G2, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 CSNK1G2, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 CSNK1G2, LENG8, 2408 more genes
    nsv3914351copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555 CSNK1G2, SEMA6B, 299 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 CSNK1G2, POLR2E, 283 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 CSNK1G2, BSG, 217 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 CSNK1G2, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 CSNK1G2, MRPL54, 198 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 CSNK1G2, AZU1, 159 more genes
    nsv3909324copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877 CSNK1G2, LOC105372234, 152 more genes
    nsv3915373copy number variation1nstd102humanPathogenic NCBI36 chr19: 1,516,574-4,059,126 , GRCh37 chr19: 1,565,574-4,108,126 , GRCh38 chr19: 1,565,575-4,108,128 CSNK1G2, LOC100419704, 104 more genes
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