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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147629copy number variation1nstd232human GRCh37.p13 chr2: 48,060,019-48,060,101 , GRCh38.p12 chr2: 47,832,880-47,832,962 FBXO11
    nsv7144015copy number variation1nstd232human GRCh37.p13 chr2: 48,035,384-48,035,464 , GRCh38.p12 chr2: 47,808,245-47,808,325 FBXO11
    nsv7139722copy number variation1nstd232human GRCh37.p13 chr2: 48,033,496-48,033,588 , GRCh38.p12 chr2: 47,806,357-47,806,449 MSH6, FBXO11
    nsv7139254copy number variation1nstd232human GRCh37.p13 chr2: 48,059,817-48,059,906 , GRCh38.p12 chr2: 47,832,678-47,832,767 FBXO11
    nsv7137020copy number variation1nstd102humanUncertain significance GRCh37 chr2: 48,033,896-48,033,949 , GRCh38 chr2: 47,806,757-47,806,810 FBXO11, MSH6
    nsv7098760copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 48,040,517-48,040,609 , GRCh38 chr2: 47,813,378-47,813,470 FBXO11
    nsv7096888copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,030,537-48,034,014 , GRCh38.p12 chr2: 47,803,398-47,806,875 FBXO11, MSH6
    nsv7096887copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,023,023-48,033,999 , GRCh38.p12 chr2: 47,795,884-47,806,860 MSH6, RPL36AP15, 1 more genes
    nsv7096886copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,010,373-48,034,014 , GRCh38.p12 chr2: 47,783,234-47,806,875 MSH6, RPL36AP15, 1 more genes
    nsv7096666copy number variation1nstd102humanUncertain significance GRCh37 chr2: 48,065,978-48,132,859 , GRCh38.p12 chr2: 47,838,839-47,905,720 FBXO11, RPS27AP7, 1 more genes
    nsv7096665copy number variation1nstd102humanUncertain significance GRCh37 chr2: 48,036,277-48,132,859 , GRCh38.p12 chr2: 47,809,138-47,905,720 LOC100506235, FBXO11, 1 more genes
    nsv7096664copy number variation1nstd102humanPathogenic GRCh37 chr2: 48,018,056-48,032,572 , GRCh38.p12 chr2: 47,790,917-47,805,433 FBXO11, MSH6, 1 more genes
    nsv7093550insertion1nstd102humanUncertain significance GRCh38 chr2: 47,806,660-47,806,660 , GRCh37 chr2: 48,033,799-48,033,799 MSH6, FBXO11
    nsv6675841copy number variation1nstd229human GRCh38 chr2: 47,814,816-47,815,156 , GRCh37.p13 chr2: 48,041,955-48,042,295 FBXO11
    nsv6674981copy number variation1nstd229human GRCh38 chr2: 47,856,438-47,891,358 , GRCh37.p13 chr2: 48,083,577-48,118,497 FBXO11, RPS27AP7
    nsv6673150copy number variation1nstd229human GRCh38 chr2: 47,883,980-47,887,487 , GRCh37.p13 chr2: 48,111,119-48,114,626 RPS27AP7, FBXO11
    nsv6671528copy number variation1nstd229human GRCh38 chr2: 47,863,249-47,874,470 , GRCh37.p13 chr2: 48,090,388-48,101,609 FBXO11
    nsv6671504copy number variation1nstd229human GRCh38 chr2: 47,792,610-47,806,680 , GRCh37.p13 chr2: 48,019,749-48,033,819 FBXO11, MSH6, 1 more genes
    nsv6667166copy number variation1nstd229human GRCh38 chr2: 47,867,701-47,870,500 , GRCh37.p13 chr2: 48,094,840-48,097,639 FBXO11
    nsv6665645copy number variation1nstd229human GRCh38 chr2: 47,893,852-47,896,905 , GRCh37.p13 chr2: 48,120,991-48,124,044 FBXO11
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