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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6635089copy number variation1nstd227human GRCh37 chr5: 120,209,700-120,792,844 , GRCh38.p12 chr5: 120,874,005-121,457,149 LOC102467226
    nsv6635895copy number variation1nstd227human GRCh37 chr7: 110,376,327-110,665,997 , GRCh38.p12 chr7: 110,736,271-111,025,941 IMMP2L
    nsv6635304copy number variation1nstd227human GRCh37 chr9: 11,649,257-11,937,390 , GRCh38.p12 chr9: 11,649,257-11,937,390 LOC101929446
    nsv6635360copy number variation1nstd227human GRCh37 chr2: 212,913,183-213,183,696 , GRCh38.p12 chr2: 212,048,458-212,318,971 ERBB4
    nsv6635749copy number variation2nstd227human GRCh37 chr2: 35,819,686-36,087,642 , GRCh38.p12 chr2: 35,594,620-35,862,576 MRPL50P1
    nsv6635649copy number variation1nstd227human GRCh37 chr18: 64,084,918-64,334,903 , GRCh38.p12 chr18: 66,417,681-66,667,666 CDH19
    nsv6635236copy number variation1nstd227human GRCh37 chr9: 11,656,743-11,903,938 , GRCh38.p12 chr9: 11,656,743-11,903,938 LOC101929446
    nsv6635687copy number variation1nstd227human GRCh37 chr9: 11,525,541-11,759,484 , GRCh38.p12 chr9: 11,525,541-11,759,484 LOC105375975
    nsv6635845copy number variation1nstd227human GRCh37 chr4: 44,396,930-44,607,572 , GRCh38.p12 chr4: 44,394,913-44,605,555 KCTD8
    nsv6635231copy number variation1nstd227human GRCh37 chr8: 137,677,675-137,857,327 , GRCh38.p12 chr8: 136,665,432-136,845,084 LINC02055
    nsv6635701copy number variation1nstd227human GRCh37 chr8: 137,679,805-137,857,327 , GRCh38.p12 chr8: 136,667,562-136,845,084 LINC02055
    nsv6635658copy number variation5nstd227human GRCh37 chr8: 137,682,484-137,857,327 , GRCh38.p12 chr8: 136,670,241-136,845,084 LINC02055
    nsv6634756copy number variation1nstd227human GRCh37 chr8: 137,677,896-137,852,251 , GRCh38.p12 chr8: 136,665,653-136,840,008 LINC02055
    nsv6635729copy number variation1nstd227human GRCh37 chr3: 60,084,924-60,248,418 , GRCh38.p12 chr3: 60,099,198-60,262,690 FHIT
    nsv6635150copy number variation1nstd227human GRCh37 chr11: 90,859,313-91,019,763 , GRCh38.p12 chr11: 91,126,145-91,286,595 LINC02748
    nsv6635702copy number variation1nstd227human GRCh37 chr7: 111,180,544-111,339,228 , GRCh38.p12 chr7: 111,540,488-111,699,172 IMMP2L
    nsv6634957copy number variation1nstd227human GRCh37 chr6: 75,018,941-75,175,449 , GRCh38.p12 chr6: 74,309,225-74,465,733 LOC101928516
    nsv6635207copy number variation1nstd227human GRCh37 chr17: 50,508,394-50,662,136 , GRCh38.p12 chr17: 52,431,034-52,584,776 , GRCh38.p12 chr17|NW_017363818.1: 1-150,600 LINC01982
    nsv6635318copy number variation1nstd227human GRCh37 chr7: 111,053,822-111,199,771 , GRCh38.p12 chr7: 111,413,766-111,559,715 IMMP2L
    nsv6635313copy number variation1nstd227human GRCh37 chr7: 110,892,226-111,025,948 , GRCh38.p12 chr7: 111,252,170-111,385,892 IMMP2L
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