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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5886884copy number variation1nstd209human GRCh38 chr1: 21,461,252-21,461,315 , GRCh37.p13 chr1: 21,787,745-21,787,808 NBPF3
    nsv5884852copy number variation1nstd209human GRCh38 chr1: 21,467,007-21,471,623 , GRCh37.p13 chr1: 21,793,500-21,798,116 NBPF3
    nsv5884014copy number variation1nstd209human GRCh38 chr1: 21,452,961-21,453,133 , GRCh37.p13 chr1: 21,779,454-21,779,626 NBPF3
    nsv5877202copy number variation1nstd209human GRCh38 chr1: 21,459,925-21,460,196 , GRCh37.p13 chr1: 21,786,418-21,786,689 NBPF3, PFN1P10
    nsv5719302mobile element insertion1nstd211human GRCh38 chr1: 21,477,619-21,477,619 , GRCh37.p13 chr1: 21,804,112-21,804,112 NBPF3
    nsv5607445insertion1nstd207human GRCh38 chr1: 21,470,069-21,470,069 , GRCh37.p13 chr1: 21,796,562-21,796,562 NBPF3
    nsv5583961copy number variation1nstd207human GRCh38 chr1: 21,450,375-21,450,773 , GRCh37.p13 chr1: 21,776,868-21,777,266 NBPF3
    nsv5583479copy number variation1nstd207human GRCh38 chr1: 21,461,252-21,461,315 , GRCh37.p13 chr1: 21,787,745-21,787,808 NBPF3
    nsv5574366copy number variation1nstd207human GRCh38 chr1: 21,459,925-21,460,196 , GRCh37.p13 chr1: 21,786,418-21,786,689 NBPF3, PFN1P10
    nsv5569495copy number variation1nstd207human GRCh38 chr1: 21,457,370-21,457,427 , GRCh37.p13 chr1: 21,783,863-21,783,920 NBPF3, PFN1P10
    nsv5555662sequence alteration1nstd206human GRCh38 chr1: 21,427,504-21,480,432 , GRCh37.p13 chr1: 21,753,997-21,806,925 NBPF3, NBPF2P, 3 more genes
    nsv5429685copy number variation1nstd206human GRCh38 chr1: 21,452,866-21,453,118 , GRCh37.p13 chr1: 21,779,359-21,779,611 NBPF3
    nsv5427499copy number variation1nstd206human GRCh38 chr1: 21,466,967-21,471,664 , GRCh37.p13 chr1: 21,793,460-21,798,157 NBPF3
    nsv5426505copy number variation1nstd206human GRCh38 chr1: 21,459,927-21,460,197 , GRCh37.p13 chr1: 21,786,420-21,786,690 NBPF3, PFN1P10
    nsv5422499copy number variation1nstd206human GRCh38 chr1: 21,461,252-21,461,316 , GRCh37.p13 chr1: 21,787,745-21,787,809 NBPF3
    nsv5420067copy number variation1nstd206human GRCh38 chr1: 21,442,532-21,443,080 , GRCh37.p13 chr1: 21,769,025-21,769,573 NBPF3
    nsv5419287copy number variation1nstd206human GRCh38 chr1: 21,452,962-21,453,134 , GRCh37.p13 chr1: 21,779,455-21,779,627 NBPF3
    nsv5349088translocation1nstd200human GRCh38 chr1: 21,461,252-21,461,252 , GRCh38 chr1: 21,461,316-21,461,316 , GRCh37.p13 chr1: 21,787,745-21,787,745 , GRCh37.p13 chr1: 21,787,809-21,787,809 NBPF3
    nsv5349087translocation1nstd200human GRCh38 chr1: 21,453,134-21,453,134 , GRCh38 chr1: 21,452,962-21,452,962 , GRCh37.p13 chr1: 21,779,455-21,779,455 , GRCh37.p13 chr1: 21,779,627-21,779,627 NBPF3
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