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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 MIR484, NDE1, 37 more genes
    nsv7148105copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,475,455-16,308,356 , GRCh38.p12 chr16: 15,381,598-16,214,499 , GRCh38.p12 chr16|NT_187607.1: 1,039,549-1,872,496 NDE1, RPL15P20, 15 more genes
    nsv7148099copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,125,542-16,388,672 , GRCh38.p12 chr16: 15,031,685-16,294,815 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,952,820 LOC100505915, ABCC1, 28 more genes
    nsv7148091copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,853,752-16,666,672 , GRCh38.p12 chr16: 14,759,895-16,572,815 RPL17P40, PKD1P3-NPIPA1, 54 more genes
    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
    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
    nsv7093396copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,927,709-16,484,731 , GRCh38.p12 chr16: 14,833,852-16,390,874 ABCC6, ABCC1, 50 more genes
    nsv7076939inversion1nstd229human GRCh38 chr16: 15,569,413-22,730,334 , GRCh37.p13 chr16: 15,663,270-22,741,655 ACSM5P1, RNU6-213P, 154 more genes
    nsv7067918inversion1nstd229human GRCh38 chr16: 14,867,200-18,528,889 , GRCh37.p13 chr16: 14,961,057-18,540,211 NPIPA1, NDE1, 80 more genes
    nsv7064706inversion1nstd229human GRCh38 chr16: 15,840,551-16,214,594 , GRCh37.p13 chr16: 15,934,408-16,308,451 ABCC6, LOC107984869, 7 more genes
    nsv7059035inversion1nstd229human GRCh38 chr16: 15,565,040-16,913,283 , GRCh37.p13 chr16: 15,658,897-17,007,140 PKD1P2, MIR3179-2, 25 more genes
    nsv6976521copy number variation1nstd229human GRCh38 chr16: 15,862,618-15,865,730 , GRCh37.p13 chr16: 15,956,475-15,959,587 CEP20
    nsv6971119copy number variation1nstd229human GRCh38 chr16: 15,882,336-15,930,427 , GRCh37.p13 chr16: 15,976,193-16,024,284 LOC107984869, CEP20, 1 more genes
    nsv6969071copy number variation1nstd229human GRCh38 chr16: 15,886,341-15,895,515 , GRCh37.p13 chr16: 15,980,198-15,989,372 CEP20
    nsv6967585copy number variation1nstd229human GRCh38 chr16: 14,928,133-16,326,551 , GRCh37.p13 chr16: 15,021,990-16,420,408 NPIPA5, PKD1P6, 39 more genes
    nsv6638040copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,509,407-16,309,046 , GRCh38.p12 chr16: 15,415,550-16,215,189 , GRCh38.p12 chr16|NT_187607.1: 1,073,529-1,873,186 ABCC6, ABCC1, 13 more genes
    nsv6637991copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,316,939-18,770,833 , GRCh38.p12 chr16: 15,223,082-18,759,511 ABCC6, ABCC1, 58 more genes
    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
    nsv6637905copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 15,509,407-16,527,476 , GRCh38.p12 chr16: 15,415,550-16,433,619 , GRCh38.p12 chr16|NT_187607.1: 1,073,529-2,094,665 ABCC6, ABCC1, 24 more genes
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