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Items: 9

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    Number of Variants: 9

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv897372copy number variation8nstd71human NCBI36 chr11: 48,676,083-48,879,221 , GRCh37.p13 chr11: 48,719,507-48,922,645 , GRCh38.p12 chr11: 48,697,955-48,901,093 ANKRD33BP2
    nsv890779copy number variation5nstd71human NCBI36 chr8: 39,356,825-39,473,097 , GRCh37.p13 chr8: 39,237,668-39,353,940 , GRCh38.p12 chr8: 39,380,149-39,496,421 ADAM3A, ADAM5
    nsv893265copy number variation25nstd71human NCBI36 chr9: 43,609,749-43,730,292 , GRCh37.p13 chr9: 43,669,753-43,790,296 , GRCh38.p12 chr9: 42,024,093-42,144,636 CNTNAP3B, LOC100420440
    nsv900898copy number variation17nstd71human NCBI36 chr13: 91,503,980-91,546,939 , GRCh37.p13 chr13: 92,705,979-92,748,938 , GRCh38.p12 chr13: 92,053,726-92,096,685 RNU4ATAC3P, GPC5
    nsv911348copy number variation463nstd71human NCBI36 chr19: 20,386,247-20,520,617 , GRCh37.p13 chr19|NW_003571053.2: 329,860-463,224 , GRCh37.p13 chr19: 20,522,409-20,728,777 , GRCh38.p12 chr19: 20,411,600-20,545,971 BNIP3P23, LOC105372317, 4 more genes
    nsv906275copy number variation1nstd71human NCBI36 chr16: 32,445,732-32,475,100 , GRCh37.p13 chr16: 32,538,231-32,567,599 , GRCh38.p12 chr16: 32,526,910-32,556,278 0
    nsv893608copy number variation1nstd71human NCBI36 chr9: 98,946,366-99,044,949 , GRCh37.p13 chr9: 99,906,545-100,005,128 , GRCh38.p12 chr9: 97,144,263-97,242,846 SUGT1P4-STRA6LP-CCDC180, ZNF322P1, 7 more genes
    nsv896955copy number variation127nstd71human NCBI36 chr11: 5,828,407-5,911,385 , GRCh37.p13 chr11: 5,871,831-5,954,809 , GRCh38.p12 chr11: 5,850,601-5,933,579 OR52E7P, OR52E4, 4 more genes
    nsv901292copy number variation51nstd71human NCBI36 chr14: 19,261,709-19,486,339 , GRCh37.p13 chr14: 20,191,869-20,416,499 , GRCh38.p12 chr14: 19,723,710-19,948,340 OR4N2, OR4Q3, 11 more genes
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