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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7012127copy number variation1nstd229human GRCh38 chr18: 2,876,020-2,879,744 , GRCh37.p13 chr18: 2,876,018-2,879,742 EMILIN2
    nsv6998709copy number variation1nstd229human GRCh38 chr18: 2,899,400-2,901,781 , GRCh37.p13 chr18: 2,899,398-2,901,779 EMILIN2
    nsv7012652copy number variation1nstd229human GRCh38 chr18: 2,884,307-2,885,575 , GRCh37.p13 chr18: 2,884,305-2,885,573 EMILIN2
    nsv7013692copy number variation1nstd229human GRCh38 chr18: 2,913,283-2,914,484 , GRCh37.p13 chr18: 2,913,281-2,914,482 EMILIN2
    nsv6999350copy number variation1nstd229human GRCh38 chr18: 2,876,495-2,876,642 , GRCh37.p13 chr18: 2,876,493-2,876,640 EMILIN2
    nsv6526346copy number variation1nstd223human GRCh38 chr18: 2,876,037-2,879,736 , GRCh37.p13 chr18: 2,876,035-2,879,734 EMILIN2
    nsv6521642copy number variation1nstd223human GRCh38 chr18: 2,848,283-2,849,525 , GRCh37.p13 chr18: 2,848,281-2,849,523 EMILIN2
    nsv6533797copy number variation1nstd223human GRCh38 chr18: 2,884,312-2,885,544 , GRCh37.p13 chr18: 2,884,310-2,885,542 EMILIN2
    nsv5526372copy number variation1nstd206human GRCh38 chr18: 2,905,756-2,914,637 , GRCh37.p13 chr18: 2,905,754-2,914,635 EMILIN2
    nsv5517134copy number variation1nstd206human GRCh38 chr18: 2,848,286-2,849,525 , GRCh37.p13 chr18: 2,848,284-2,849,523 EMILIN2
    nsv5528353copy number variation1nstd206human GRCh38 chr18: 2,884,285-2,885,572 , GRCh37.p13 chr18: 2,884,283-2,885,570 EMILIN2
    nsv6145186copy number variation1nstd206human GRCh38 chr18: 2,876,497-2,876,927 , GRCh37.p13 chr18: 2,876,495-2,876,925 EMILIN2
    nsv5526647copy number variation1nstd206human GRCh38 chr18: 2,858,526-2,858,828 , GRCh37.p13 chr18: 2,858,524-2,858,826 EMILIN2
    nsv5518524copy number variation1nstd206human GRCh38 chr18: 2,876,495-2,876,642 , GRCh37.p13 chr18: 2,876,493-2,876,640 EMILIN2
    nsv6306351copy number variation1nstd186human GRCh37 chr18: 2,876,495-2,876,925 , GRCh38.p12 chr18: 2,876,497-2,876,927 EMILIN2
    nsv6124702copy number variation1nstd186human GRCh37 chr18: 2,876,493-2,876,640 , GRCh38.p12 chr18: 2,876,495-2,876,642 EMILIN2
    nsv4647210copy number variation3nstd186human GRCh37 chr18: 2,876,495-2,876,640 , GRCh38.p12 chr18: 2,876,497-2,876,642 EMILIN2
    nsv6274939copy number variation1nstd214human GRCh38 chr18: 2,876,495-2,876,641 , GRCh37.p13 chr18: 2,876,493-2,876,639 EMILIN2
    nsv6032900copy number variation1nstd212human GRCh38 chr18: 2,858,505-2,858,726 , GRCh37.p13 chr18: 2,858,503-2,858,724 EMILIN2
    nsv6035468copy number variation1nstd212human GRCh38 chr18: 2,876,494-2,876,642 , GRCh37.p13 chr18: 2,876,492-2,876,640 EMILIN2
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