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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888921copy number variation1nstd102humanUncertain significance GRCh37 chr2: 223,917,655-224,104,275 , GRCh38.p12 chr2: 223,052,937-223,239,557 KCNE4, LOC105373905, 1 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 KCNE4, DAZAP2P1, 2991 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 KCNE4, LOC105373947, 357 more genes
    nsv3881953copy number variation1nstd102humanPathogenic GRCh37 chr2: 223,378,640-232,061,074 , GRCh38.p12 chr2: 222,513,921-231,196,360 KCNE4, LOC105373925, 112 more genes
    nsv3873368copy number variation1nstd102humanPathogenic GRCh37 chr2: 218,813,434-227,450,699 , GRCh38.p12 chr2: 217,948,711-226,585,983 KCNE4, ARPC2, 163 more genes
    nsv6112757copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,056,891-227,164,817 , GRCh38.p12 chr2: 219,192,169-226,300,101 KCNE4, DES, 100 more genes
    nsv3906433copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,946,342-226,295,024 , GRCh38 chr2: 219,081,620-225,430,308 , NCBI36 chr2: 219,654,586-226,003,268 KCNE4, HIGD1AP4, 102 more genes
    nsv3873167copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,614,743-225,587,770 , GRCh38.p12 chr2: 219,750,021-224,723,053 KCNE4, SCG2, 59 more genes
    nsv3888475copy number variation1nstd102humanPathogenic GRCh37 chr2: 221,439,250-226,170,404 , GRCh38.p12 chr2: 220,574,529-225,305,687 KCNE4, FAM124B, 55 more genes
    nsv3879172copy number variation1nstd102humanPathogenic GRCh37 chr2: 220,608,798-224,217,756 , GRCh38.p12 chr2: 219,744,076-223,353,038 KCNE4, LOC100419511, 43 more genes
    nsv6315345copy number variation1nstd102humanPathogenic GRCh37 chr2: 222,902,251-226,084,516 , GRCh38.p12 chr2: 222,037,532-225,219,799 KCNE4, LOC105373911, 43 more genes
    nsv3890905copy number variation1nstd102humanPathogenic GRCh38 chr2: 221,663,502-224,426,183 , NCBI36 chr2: 222,236,466-224,999,144 , GRCh37 chr2: 222,528,222-225,290,900 KCNE4, LOC105373900, 41 more genes
    nsv4728510copy number variation1nstd102humanPathogenic GRCh37 chr2: 222,621,434-224,754,689 , GRCh38.p12 chr2: 221,756,714-223,889,972 KCNE4, LOC105373905, 32 more genes
    nsv6313567copy number variation1nstd102humanPathogenic GRCh37 chr2: 222,828,685-224,451,613 , GRCh38.p12 chr2: 221,963,966-223,586,895 KCNE4, LOC105373905, 26 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 KCNE4, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 KCNE4, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 KCNE4, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 KCNE4, MTND2P22, 3724 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 KCNE4, LOC105376755, 1013 more genes
    nsv3890898copy number variation1nstd102humanPathogenic GRCh38 chr2: 188,818,195-242,065,208 , NCBI36 chr2: 189,391,166-242,656,032 , GRCh37 chr2: 189,682,921-243,007,359 KCNE4, LOC105373909, 901 more genes
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