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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6628914copy number variation179nstd224human GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491 NLGN1
    nsv6632402copy number variation1nstd224human GRCh37 chr7: 88,657,093-89,118,409 , GRCh38.p12 chr7: 89,027,779-89,489,095 LOC105375387, ZNF804B
    nsv6630884copy number variation168nstd224human GRCh37 chr5: 814,876-825,329 , GRCh38.p12 chr5: 814,761-825,214 ZDHHC11, SPCS2P3
    nsv6633598copy number variation154nstd224human GRCh37 chr9: 140,173,637-140,196,334 , GRCh38.p12 chr9: 137,279,185-137,301,882 NRARP, TOR4A
    nsv6625917copy number variation63nstd224human GRCh37 chr1: 17,216,331-17,266,464 , GRCh38.p12 chr1: 16,889,836-16,939,969 CROCC, LOC105376805, 3 more genes
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