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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130101insertion1nstd186human GRCh37 chr16: 84,030,649-84,030,655 , GRCh38.p12 chr16: 83,997,044-83,997,050 NECAB2
    nsv5973943insertion1nstd209human GRCh38 chr16: 83,997,050-83,997,050 , GRCh37.p13 chr16: 84,030,655-84,030,655 NECAB2
    nsv5941925copy number variation1nstd209human GRCh38 chr16: 83,974,915-83,975,094 , GRCh37.p13 chr16: 84,008,520-84,008,699 NECAB2
    nsv5673088copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,005,756-84,164,926 , GRCh38.p12 chr16: 83,972,151-84,131,321 MBTPS1, NECAB2, 4 more genes
    nsv5655142insertion1nstd207human GRCh38 chr16: 83,975,004-83,975,004 , GRCh37.p13 chr16: 84,008,609-84,008,609 NECAB2
    nsv5651429insertion1nstd207human GRCh38 chr16: 83,975,163-83,975,163 , GRCh37.p13 chr16: 84,008,768-84,008,768 NECAB2
    nsv5646075insertion1nstd207human GRCh38 chr16: 83,997,579-83,997,579 , GRCh37.p13 chr16: 84,031,184-84,031,184 NECAB2
    nsv5553415insertion1nstd206human GRCh38 chr16: 83,997,044-83,997,050 , GRCh37.p13 chr16: 84,030,649-84,030,655 NECAB2
    nsv5541832insertion1nstd206human GRCh38 chr16: 83,998,984-83,999,009 , GRCh37.p13 chr16: 84,032,589-84,032,614 NECAB2
    nsv5535126insertion1nstd206human GRCh38 chr16: 83,997,663-83,997,669 , GRCh37.p13 chr16: 84,031,268-84,031,274 NECAB2
    nsv5526880copy number variation1nstd206human GRCh38 chr16: 83,956,448-84,018,129 , GRCh37.p13 chr16: 83,990,053-84,051,734 SLC38A8, OSGIN1, 1 more genes
    nsv5521945copy number variation1nstd206human GRCh38 chr16: 83,998,958-83,999,019 , GRCh37.p13 chr16: 84,032,563-84,032,624 NECAB2
    nsv5514824copy number variation1nstd206human GRCh38 chr16: 83,977,266-83,977,348 , GRCh37.p13 chr16: 84,010,871-84,010,953 NECAB2
    nsv5358454translocation1nstd200human GRCh38 chr16: 83,981,663-83,981,663 , GRCh38 chr16: 83,981,744-83,981,744 , GRCh37.p13 chr16: 84,015,349-84,015,349 , GRCh37.p13 chr16: 84,015,268-84,015,268 NECAB2
    nsv5307865copy number variation1nstd204human GRCh38.p13 chr16: 84,002,270-84,002,796 , GRCh37.p13 chr16: 84,035,875-84,036,401 NECAB2
    nsv5013484copy number variation1nstd200human GRCh38 chr16: 83,973,209-83,973,423 , GRCh37.p13 chr16: 84,006,814-84,007,028 NECAB2
    nsv5009835copy number variation1nstd200human GRCh38 chr16: 84,002,975-84,003,995 , GRCh37.p13 chr16: 84,036,580-84,037,600 NECAB2
    nsv5009834copy number variation1nstd200human GRCh38 chr16: 84,002,912-84,009,815 , GRCh37.p13 chr16: 84,036,517-84,043,420 NECAB2, SLC38A8
    nsv5009833copy number variation1nstd200human GRCh38 chr16: 83,999,858-84,027,496 , GRCh37.p13 chr16: 84,033,463-84,061,101 SLC38A8, NECAB2
    nsv5009832copy number variation1nstd200human GRCh38 chr16: 83,999,150-83,999,276 , GRCh37.p13 chr16: 84,032,755-84,032,881 NECAB2
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