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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147815copy number variation1nstd232human GRCh37.p13 chr1: 21,787,745-21,787,808 , GRCh38.p12 chr1: 21,461,252-21,461,315 NBPF3
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7057212inversion1nstd229human GRCh38 chr1: 21,399,935-21,488,253 , GRCh37.p13 chr1: 21,726,428-21,814,746 NBPF3, HS6ST1P1, 5 more genes
    nsv7055295inversion1nstd229human GRCh38 chr1: 20,526,331-21,860,622 , GRCh37.p13 chr1: 20,852,824-22,187,115 USP48, ECE1, 31 more genes
    nsv6647250copy number variation1nstd229human GRCh38 chr1: 21,467,010-21,471,622 , GRCh37.p13 chr1: 21,793,503-21,798,115 NBPF3
    nsv6647249copy number variation1nstd229human GRCh38 chr1: 21,427,058-21,469,081 , GRCh37.p13 chr1: 21,753,551-21,795,574 PFN1P10, HS6ST1P1, 3 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6647180copy number variation1nstd229human GRCh38 chr1: 21,461,252-21,461,316 , GRCh37.p13 chr1: 21,787,745-21,787,809 NBPF3
    nsv6647122copy number variation1nstd229human GRCh38 chr1: 21,484,305-21,490,604 , GRCh37.p13 chr1: 21,810,798-21,817,097 NBPF3
    nsv6647121copy number variation1nstd229human GRCh38 chr1: 21,473,006-21,479,440 , GRCh37.p13 chr1: 21,799,499-21,805,933 NBPF3
    nsv6647120copy number variation1nstd229human GRCh38 chr1: 21,459,927-21,460,197 , GRCh37.p13 chr1: 21,786,420-21,786,690 NBPF3, PFN1P10
    nsv6646737copy number variation1nstd229human GRCh38 chr1: 21,474,280-21,477,047 , GRCh37.p13 chr1: 21,800,773-21,803,540 NBPF3
    nsv6646736copy number variation1nstd229human GRCh38 chr1: 21,452,408-21,452,799 , GRCh37.p13 chr1: 21,778,901-21,779,292 NBPF3
    nsv6646735copy number variation1nstd229human GRCh38 chr1: 21,432,830-21,435,151 , GRCh37.p13 chr1: 21,759,323-21,761,644 CROCCP5, NBPF3
    nsv6328861copy number variation1nstd223human GRCh38 chr1: 21,459,927-21,460,197 , GRCh37.p13 chr1: 21,786,420-21,786,690 PFN1P10, NBPF3
    nsv6322623copy number variation1nstd223human GRCh38 chr1: 21,452,408-21,452,799 , GRCh37.p13 chr1: 21,778,901-21,779,292 NBPF3
    nsv6319320copy number variation1nstd223human GRCh38 chr1: 21,390,104-21,479,264 , GRCh37.p13 chr1: 21,716,597-21,805,757 NBPF3, PDE4DIPP10, 6 more genes
    nsv6219051insertion1nstd214human GRCh38 chr1: 21,459,927-21,459,927 , GRCh37.p13 chr1: 21,786,420-21,786,420 PFN1P10, NBPF3
    nsv6166214copy number variation1nstd214human GRCh38 chr1: 21,461,252-21,461,315 , GRCh37.p13 chr1: 21,787,745-21,787,808 NBPF3
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