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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
    nsv3904451copy number variation1nstd102humanBenign GRCh37 chr16: 90,070,169-90,074,201 , GRCh38.p12 chr16: 90,003,761-90,007,793 DBNDD1
    nsv3894637copy number variation1nstd102humanBenign GRCh37 chr16: 90,070,169-90,074,001 , GRCh38.p12 chr16: 90,003,761-90,007,593 DBNDD1
    nsv3913454copy number variation1nstd102humanBenign NCBI36 chr16: 88,614,352-88,675,901 , GRCh37 chr16: 90,086,851-90,148,400 , GRCh38 chr16: 90,020,443-90,081,992 DBNDD1, GAS8, 3 more genes
    nsv3890896copy number variation1nstd102humanBenign GRCh37 chr16: 90,072,265-90,113,107 , GRCh38.p12 chr16: 90,005,857-90,046,699 DBNDD1, GAS8, 2 more genes
    nsv3923070copy number variation1nstd102humanLikely benign NCBI36 chr16: 88,614,352-88,632,928 , GRCh37 chr16: 90,086,851-90,105,427 , GRCh38 chr16: 90,020,443-90,039,019 DBNDD1, GAS8, 2 more genes
    nsv3895017copy number variation1nstd102humanBenign GRCh37 chr16: 90,053,048-90,102,384 , GRCh38.p12 chr16: 89,986,640-90,035,976 DBNDD1, GAS8-AS1, 2 more genes
    nsv4457411copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,081,509-90,155,062 , GRCh38.p12 chr16: 90,015,101-90,088,654 DBNDD1, PRDM7, 3 more genes
    nsv3911537copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,086,998-90,148,393 , GRCh38 chr16: 90,020,590-90,081,985 , NCBI36 chr16: 88,614,499-88,675,894 DBNDD1, PRDM7, 3 more genes
    nsv4457748copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,080,098-90,134,747 , GRCh38.p12 chr16: 90,013,690-90,068,339 DBNDD1, PRDM7, 3 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 DBNDD1, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 DBNDD1, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 DBNDD1, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 DBNDD1, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 DBNDD1, 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 DBNDD1, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 DBNDD1, 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 DBNDD1, CFAP69P1, 716 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 DBNDD1, 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 DBNDD1, LOC105376772, 527 more genes
    nsv3910304copy number variation1nstd102humanPathogenic NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403 DBNDD1, MC1R, 528 more genes
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