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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3908259copy number variation1nstd102humanBenign GRCh37 chr9: 8,247,628-8,484,240 , GRCh38.p12 chr9: 8,247,628-8,484,240 PTPRD
    nsv4728802copy number variation1nstd102humanLikely benign GRCh37 chr9: 10,292,536-10,491,387 , GRCh38.p12 chr9: 10,292,536-10,491,387 PTPRD
    nsv3902345copy number variation1nstd102humanBenign GRCh37 chr9: 9,816,063-9,954,379 , GRCh38.p12 chr9: 9,816,063-9,954,379 PTPRD
    nsv3900299copy number variation1nstd102humanBenign GRCh37 chr9: 8,903,857-9,032,105 , GRCh38.p12 chr9: 8,903,857-9,032,105 PTPRD
    nsv3896457copy number variation1nstd102humanBenign GRCh37 chr9: 9,562,254-9,687,487 , GRCh38.p12 chr9: 9,562,254-9,687,487 PTPRD
    nsv3911763copy number variation1nstd102humanBenign NCBI36 chr9: 8,893,382-9,004,802 , GRCh38 chr9: 8,903,382-9,014,802 , GRCh37 chr9: 8,903,382-9,014,802 PTPRD
    nsv3905954copy number variation1nstd102humanBenign GRCh37 chr9: 9,904,274-9,979,990 , GRCh38.p12 chr9: 9,904,274-9,979,990 PTPRD
    nsv3896610copy number variation1nstd102humanLikely benign GRCh37 chr9: 9,919,638-9,990,269 , GRCh38.p12 chr9: 9,919,638-9,990,269 PTPRD
    nsv3913500copy number variation1nstd102humanBenign NCBI36 chr9: 8,274,068-8,321,541 , GRCh38 chr9: 8,284,068-8,331,541 , GRCh37 chr9: 8,284,068-8,331,541 PTPRD
    nsv3899038copy number variation1nstd102humanLikely benign GRCh37 chr9: 8,802,640-8,836,439 , GRCh38.p12 chr9: 8,802,640-8,836,439 PTPRD
    nsv3901057copy number variation1nstd102humanBenign GRCh37 chr9: 9,711,904-9,733,974 , GRCh38.p12 chr9: 9,711,904-9,733,974 PTPRD
    nsv3906217copy number variation1nstd102humanBenign GRCh37 chr9: 10,394,286-10,405,076 , GRCh38.p12 chr9: 10,394,286-10,405,076 PTPRD
    nsv3904085copy number variation1nstd102humanBenign GRCh37 chr9: 8,635,810-8,641,791 , GRCh38.p12 chr9: 8,635,810-8,641,791 PTPRD
    nsv3891548copy number variation1nstd102humanBenign GRCh37 chr9: 8,635,810-8,641,684 , GRCh38.p12 chr9: 8,635,810-8,641,684 PTPRD
    nsv3906840copy number variation1nstd102humanBenign GRCh37 chr9: 9,340,617-9,342,118 , GRCh38.p12 chr9: 9,340,617-9,342,118 PTPRD
    nsv3899472copy number variation1nstd102humanBenign GRCh37 chr9: 8,640,921-8,641,739 , GRCh38.p12 chr9: 8,640,921-8,641,739 PTPRD
    nsv3896989copy number variation1nstd102humanBenign GRCh37 chr9: 9,340,617-9,340,891 , GRCh38.p12 chr9: 9,340,617-9,340,891 PTPRD
    nsv3895113copy number variation1nstd102humanBenign GRCh37 chr9: 9,340,701-9,340,891 , GRCh38.p12 chr9: 9,340,701-9,340,891 PTPRD
    nsv3919576copy number variation1nstd102humanBenign GRCh38 chr9: 10,249,116-10,340,720 , GRCh37 chr9: 10,249,116-10,340,720 , NCBI36 chr9: 10,239,116-10,330,720 PTPRD
    nsv3904516copy number variation1nstd102humanBenign GRCh37 chr9: 10,254,449-10,318,512 , GRCh38.p12 chr9: 10,254,449-10,318,512 PTPRD
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