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Items: 1 to 20 of 64

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3894312copy number variation1nstd102humanBenign GRCh37 chr16: 74,465,514-74,592,483 , GRCh38.p12 chr16: 74,431,616-74,558,585 GLG1, LOC107984827, 2 more genes
    nsv4456737copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,612,941-74,669,629 , GRCh38.p12 chr16: 74,579,043-74,635,731 GLG1, RFWD3, 1 more genes
    nsv7094598copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,505,051-74,695,347 , GRCh38.p12 chr16: 74,471,153-74,661,449 GLG1, RPS10P23, 2 more genes
    nsv4456429copy number variation1nstd102humanUncertain significance GRCh37 chr16: 74,456,587-74,630,675 , GRCh38.p12 chr16: 74,422,689-74,596,777 GLG1, LOC107984827, 3 more genes
    nsv3921095copy number variation1nstd102humanPathogenic NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726 GLG1, NECAB2, 219 more genes
    nsv3918168copy number variation1nstd102humanPathogenic NCBI36 chr16: 71,640,867-81,167,432 , GRCh38 chr16: 73,049,467-82,576,326 , GRCh37 chr16: 73,083,366-82,609,931 GLG1, BCAR1, 125 more genes
    nsv3917504copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,951,979-76,757,245 , NCBI36 chr16: 68,509,480-75,314,746 , GRCh38 chr16: 69,918,076-76,723,348 GLG1, TRG-GCC3-1, 137 more genes
    nsv3916803copy number variation1nstd102humanPathogenic NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298 GLG1, AP1G1, 138 more genes
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 GLG1, ZNF19, 128 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 GLG1, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 GLG1, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 GLG1, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 GLG1, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 GLG1, FTLP14, 1868 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 GLG1, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 GLG1, ATMIN, 826 more genes
    nsv3915506copy number variation1nstd102humanPathogenic NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062 GLG1, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 GLG1, LOC107984894, 613 more genes
    nsv3913913copy number variation1nstd102humanPathogenic NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393 GLG1, ATP5F1AP3, 534 more genes
    nsv3919817copy number variation1nstd102humanPathogenic NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985 GLG1, LOC105376772, 527 more genes
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