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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137121copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,819,740-16,364,041 , GRCh38.p12 chr16: 14,725,883-16,270,184 , GRCh38.p12 chr16|NT_187607.1: 266,171-1,928,187 ABCC6, ABCC1, 54 more genes
    nsv7099033copy number variation1nstd102humannot provided GRCh37 chr16: 14,619,584-14,868,417 , GRCh38.p12 chr16: 14,525,727-14,774,560 NPIPA2, LOC107984865, 7 more genes
    nsv7099031copy number variation1nstd102humanUncertain significance GRCh38 chr16: 14,683,149-16,205,174 , GRCh37.p13 chr16: 14,777,006-16,299,031 LOC100288162, LOC105371096, 43 more genes
    nsv7098843copy number variation1nstd102humanLikely pathogenic GRCh38 chr16: 14,683,149-16,536,956 , GRCh37.p13 chr16: 14,777,006-16,630,813 ABCC6, ABCC1, 56 more genes
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv7073405inversion1nstd229human GRCh38 chr16: 14,540,157-14,993,130 , GRCh37.p13 chr16: 14,634,014-15,086,987 LOC100652777, NPIPA1, 20 more genes
    nsv7068744inversion1nstd229human GRCh38 chr16: 14,595,692-15,383,928 , GRCh37.p13 chr16: 14,689,549-15,477,785 PKD1P6, NPIPA5, 32 more genes
    nsv7065280inversion1nstd229human GRCh38 chr16: 14,489,001-15,167,857 , GRCh37.p13 chr16: 14,582,858-15,261,714 NPIPA2, PARN, 31 more genes
    nsv6976360copy number variation1nstd229human GRCh38 chr16: 14,674,452-14,678,518 , GRCh37.p13 chr16: 14,768,309-14,772,375 PLA2G10
    nsv6962375copy number variation1nstd229human GRCh38 chr16: 14,671,306-14,674,862 , GRCh37.p13 chr16: 14,765,163-14,768,719 PLA2G10
    nsv6637929copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,780,544-16,330,627 , GRCh38.p12 chr16: 14,686,687-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 259,546-1,894,768 LOC102724984, ABCC6P2, 54 more genes
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6590102inversion1nstd223human GRCh38 chr16: 14,683,027-14,683,246 , GRCh37.p13 chr16: 14,776,884-14,777,103 PLA2G10
    nsv6589785inversion1nstd223human GRCh38 chr16: 14,679,807-14,680,548 , GRCh37.p13 chr16: 14,773,664-14,774,405 PLA2G10
    nsv6589687inversion1nstd223human GRCh38 chr16: 14,686,446-14,687,147 , GRCh37.p13 chr16: 14,780,303-14,781,004 PLA2G10
    nsv6589433inversion1nstd223human GRCh38 chr16: 14,685,369-14,685,715 , GRCh37.p13 chr16: 14,779,226-14,779,572 PLA2G10
    nsv6584072inversion1nstd223human GRCh38 chr16: 14,685,412-14,685,815 , GRCh37.p13 chr16: 14,779,269-14,779,672 PLA2G10
    nsv6582729inversion1nstd223human GRCh38 chr16: 14,670,773-14,671,655 , GRCh37.p13 chr16: 14,764,630-14,765,512 PLA2G10
    nsv6578798inversion1nstd223human GRCh38 chr16: 14,673,035-14,675,174 , GRCh37.p13 chr16: 14,766,892-14,769,031 PLA2G10
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