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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951650insertion1nstd209human GRCh38 chr10: 8,268,507-8,268,507 , GRCh37.p13 chr10: 8,310,470-8,310,470 LINC00708
    nsv5920474copy number variation1nstd209human GRCh38 chr10: 8,268,731-8,269,006 , GRCh37.p13 chr10: 8,310,694-8,310,969 LINC00708
    nsv5917566copy number variation1nstd209human GRCh38 chr10: 8,268,450-8,268,683 , GRCh37.p13 chr10: 8,310,413-8,310,646 LINC00708
    nsv5910697copy number variation1nstd209human GRCh38 chr10: 8,268,460-8,268,523 , GRCh37.p13 chr10: 8,310,423-8,310,486 LINC00708
    nsv5910282copy number variation1nstd209human GRCh38 chr10: 8,266,758-8,266,815 , GRCh37.p13 chr10: 8,308,721-8,308,778 LINC00708
    nsv5635915insertion1nstd207human GRCh38 chr10: 8,268,511-8,268,511 , GRCh37.p13 chr10: 8,310,474-8,310,474 LINC00708
    nsv5597386copy number variation1nstd207human GRCh38 chr10: 8,268,688-8,269,189 , GRCh37.p13 chr10: 8,310,651-8,311,152 LINC00708
    nsv5586722copy number variation1nstd207human GRCh38 chr10: 8,268,438-8,268,579 , GRCh37.p13 chr10: 8,310,401-8,310,542 LINC00708
    nsv5545238insertion1nstd206human GRCh38 chr10: 8,268,553-8,268,557 , GRCh37.p13 chr10: 8,310,516-8,310,520 LINC00708
    nsv4969520copy number variation1nstd200human GRCh38 chr10: 8,254,848-8,261,287 , GRCh37.p13 chr10: 8,296,811-8,303,250 LINC00708
    nsv4846239copy number variation1nstd200human GRCh37 chr10: 8,304,939-8,305,252 , GRCh38.p12 chr10: 8,262,976-8,263,289 LINC00708
    nsv4842344copy number variation1nstd200human GRCh37 chr10: 8,296,811-8,303,250 , GRCh38.p12 chr10: 8,254,848-8,261,287 LINC00708
    nsv4749234copy number variation1nstd199human GRCh37 chr10: 8,310,400-8,310,543 , GRCh38.p12 chr10: 8,268,437-8,268,580 LINC00708
    nsv4637053copy number variation1nstd186human GRCh37 chr10: 8,310,355-8,311,158 , GRCh38.p12 chr10: 8,268,392-8,269,195 LINC00708
    nsv4525753copy number variation1nstd166human GRCh37.p13 chr10: 8,310,355-8,311,158 , GRCh38.p12 chr10: 8,268,392-8,269,195 LINC00708
    nsv4456896copy number variation1nstd102humanUncertain significance GRCh37 chr10: 8,075,029-8,407,665 , GRCh38.p12 chr10: 8,033,066-8,365,702 LOC107984205, LOC105376394, 6 more genes
    nsv4455884copy number variation1nstd102humanPathogenic GRCh37 chr10: 8,011,156-9,996,086 , GRCh38.p12 chr10: 7,969,193-9,954,123 LOC105376396, KRT8P37, 22 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4339122sequence alteration1nstd166human GRCh37.p13 chr10: 8,298,979-8,310,371 , GRCh38.p12 chr10: 8,257,016-8,268,408 LINC00708
    nsv3940346copy number variation1nstd167human GRCh37 chr10: 8,310,401-8,310,543 , GRCh38.p12 chr10: 8,268,438-8,268,580 LINC00708
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