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Items: 12

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    Number of Variants: 12

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3113934copy number variation6nstd145human GRCh37 chr16: 55,797,365-55,832,503 , GRCh38.p12 chr16: 55,763,453-55,798,591 CES1P1
    nsv3113267copy number variation16nstd145human GRCh37 chr20: 1,561,593-1,593,574 , GRCh38.p12 chr20: 1,580,947-1,612,928 SIRPB1
    nsv3116670copy number variation2nstd145human GRCh37 chr19: 52,137,663-52,148,550 , GRCh38.p12 chr19: 51,634,410-51,645,297 SIGLEC14
    nsv3117889copy number variation1nstd145human GRCh37 chr21: 23,658,461-23,666,101 , GRCh38.p12 chr21|NW_003315968.2: 190,370-198,010 , GRCh38.p12 chr21: 22,286,141-22,293,781 LOC107985508
    nsv3115066copy number variation81nstd145human GRCh37 chr6: 19,042,250-19,049,222 , GRCh38.p12 chr6: 19,042,019-19,048,991 LOC105374958
    nsv3117147copy number variation17nstd145human GRCh37 chr8: 39,233,286-39,385,964 , GRCh38.p12 chr8: 39,375,767-39,528,445 ADAM3A, ADAM5
    nsv3112695copy number variation1nstd145human GRCh37 chr13: 34,139,882-34,144,661 , GRCh38.p12 chr13: 33,565,745-33,570,524 STARD13, LOC102723406
    nsv3112199copy number variation14nstd145human GRCh37 chr17: 39,423,253-39,433,198 , GRCh38.p12 chr17: 41,267,001-41,276,946 , GRCh38.p12 chr17|NW_003871093.1: 30,164-40,109 KRTAP9-11P, KRTAP9-7, 1 more genes
    nsv3117136copy number variation71nstd145human GRCh37 chr16: 62,545,058-62,550,573 , GRCh38.p12 chr16: 62,511,154-62,516,669 0
    nsv3113772copy number variation1nstd145human GRCh37 chr6: 103,735,326-103,740,419 , GRCh38.p12 chr6: 103,287,451-103,292,544 0
    nsv3116729copy number variation1nstd145human GRCh37 chr18: 51,205,749-51,210,311 , GRCh38.p12 chr18: 53,679,379-53,683,941 0
    nsv3115677copy number variation1nstd145human GRCh37 chr3: 70,432,971-70,435,656 , GRCh38.p12 chr3: 70,383,820-70,386,505 0
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