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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6627960copy number variation4nstd224human GRCh37 chr2: 52,407,060-52,578,154 , GRCh38.p12 chr2: 52,179,922-52,351,016 NRXN1-DT
    nsv6628116copy number variation277nstd224human GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186 SRSF7, GALM
    nsv6625811copy number variation25nstd224human GRCh37 chr1: 17,216,331-17,273,287 , GRCh38.p12 chr1: 16,889,836-16,946,792 TRN-GTT4-1, LOC105376805, 3 more genes
    nsv6631445copy number variation586nstd224human GRCh37 chr6: 67,017,543-67,044,431 , GRCh38.p12 chr6: 66,307,650-66,334,538 0
    nsv6632339copy number variation1nstd224human GRCh37 chr7: 57,481,104-57,755,757 , GRCh38.p12 chr7: 57,421,392-57,696,051 ZNF716, SAPCD2P2, 7 more genes
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