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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3874301copy number variation1nstd102humanBenign GRCh37 chr5: 76,318,206-76,325,361 , GRCh38.p12 chr5: 77,022,381-77,029,536 AGGF1
    nsv3874904copy number variation1nstd102humanBenign GRCh37 chr5: 76,326,719-76,355,468 , GRCh38.p12 chr5: 77,030,894-77,059,643 AGGF1
    nsv3880872copy number variation1nstd102humanBenign GRCh37 chr5: 76,331,387-76,359,048 , GRCh38.p12 chr5: 77,035,562-77,063,223 AGGF1
    nsv3878559copy number variation1nstd102humanBenign GRCh37 chr5: 76,331,387-76,355,468 , GRCh38.p12 chr5: 77,035,562-77,059,643 AGGF1
    nsv6777936copy number variation1nstd229human GRCh38 chr5: 77,045,857-77,049,261 , GRCh37.p13 chr5: 76,341,682-76,345,086 AGGF1
    nsv6762920copy number variation1nstd229human GRCh38 chr5: 77,032,902-77,032,937 , GRCh37.p13 chr5: 76,328,727-76,328,762 AGGF1
    nsv6016681copy number variation1nstd212human GRCh38 chr5: 77,043,056-77,043,234 , GRCh37.p13 chr5: 76,338,881-76,339,059 AGGF1
    nsv6013767copy number variation1nstd212human GRCh38 chr5: 77,042,807-77,042,957 , GRCh37.p13 chr5: 76,338,632-76,338,782 AGGF1
    nsv6001253copy number variation1nstd212human GRCh38 chr5: 77,042,405-77,042,553 , GRCh37.p13 chr5: 76,338,230-76,338,378 AGGF1
    nsv6009048copy number variation1nstd212human GRCh38 chr5: 77,043,364-77,043,500 , GRCh37.p13 chr5: 76,339,189-76,339,325 AGGF1
    nsv6005695copy number variation1nstd212human GRCh38 chr5: 77,042,765-77,042,820 , GRCh37.p13 chr5: 76,338,590-76,338,645 AGGF1
    nsv6015994copy number variation1nstd212human GRCh38 chr5: 77,042,958-77,043,012 , GRCh37.p13 chr5: 76,338,783-76,338,837 AGGF1
    nsv6017946copy number variation1nstd212human GRCh38 chr5: 77,043,488-77,043,541 , GRCh37.p13 chr5: 76,339,313-76,339,366 AGGF1
    nsv6012161copy number variation1nstd212human GRCh38 chr5: 77,042,444-77,042,497 , GRCh37.p13 chr5: 76,338,269-76,338,322 AGGF1
    nsv6002872copy number variation1nstd212human GRCh38 chr5: 77,042,814-77,042,866 , GRCh37.p13 chr5: 76,338,639-76,338,691 AGGF1
    nsv4750006copy number variation1nstd199human GRCh37 chr5: 76,338,247-76,338,301 , GRCh38.p12 chr5: 77,042,422-77,042,476 AGGF1
    nsv5579864copy number variation1nstd207human GRCh38 chr5: 77,042,651-77,043,199 , GRCh37.p13 chr5: 76,338,476-76,339,024 AGGF1
    nsv5580763copy number variation1nstd207human GRCh38 chr5: 77,042,480-77,042,671 , GRCh37.p13 chr5: 76,338,305-76,338,496 AGGF1
    nsv5580720copy number variation1nstd207human GRCh38 chr5: 77,042,787-77,042,932 , GRCh37.p13 chr5: 76,338,612-76,338,757 AGGF1
    nsv5573492copy number variation1nstd207human GRCh38 chr5: 77,043,355-77,043,481 , GRCh37.p13 chr5: 76,339,180-76,339,306 AGGF1
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