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Items: 1 to 20 of 73

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905789copy number variation1nstd102humanBenign GRCh37 chr16: 82,160,951-82,213,799 , GRCh38.p12 chr16: 82,127,346-82,180,194 MPHOSPH6
    nsv3904308copy number variation1nstd102humanBenign GRCh37 chr16: 82,165,314-82,213,799 , GRCh38.p12 chr16: 82,131,709-82,180,194 MPHOSPH6
    nsv3923955copy number variation1nstd102humanUncertain significance GRCh38 chr16: 82,163,949-82,280,684 , GRCh37 chr16: 82,197,554-82,314,289 , NCBI36 chr16: 80,755,055-80,871,790 MPHOSPH6, RN7SKP190
    nsv3913506copy number variation1nstd102humanUncertain significance NCBI36 chr16: 80,723,959-81,146,040 , GRCh37.p13 chr16: 82,166,458-82,588,539 , GRCh38.p12 chr16: 82,132,853-82,554,934 MPHOSPH6, RN7SKP190, 2 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 MPHOSPH6, 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 MPHOSPH6, BCAR1, 125 more genes
    nsv3919844copy number variation1nstd102humanPathogenic GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449 MPHOSPH6, RPL10AP12, 146 more genes
    nsv3916915copy number variation1nstd102humanPathogenic NCBI36 chr16: 77,381,848-81,846,527 , GRCh38 chr16: 78,790,450-83,255,421 , GRCh37 chr16: 78,824,347-83,289,026 MPHOSPH6, LOC100419639, 50 more genes
    nsv3917609copy number variation1nstd102humanPathogenic NCBI36 chr16: 80,344,868-84,305,898 , GRCh37 chr16: 81,787,367-85,748,397 , GRCh38 chr16: 81,753,762-85,714,791 MPHOSPH6, LOC105371376, 63 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 MPHOSPH6, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 MPHOSPH6, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 MPHOSPH6, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 MPHOSPH6, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 MPHOSPH6, 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 MPHOSPH6, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 MPHOSPH6, 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 MPHOSPH6, CFAP69P1, 716 more genes
    nsv3891306copy number variation1nstd102humanPathogenic GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261 MPHOSPH6, 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 MPHOSPH6, 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 MPHOSPH6, LOC105376772, 527 more genes
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