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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5533399copy number variation1nstd206human GRCh38 chr16: 82,163,425-82,163,482 , GRCh37.p13 chr16: 82,197,030-82,197,087 MPHOSPH6
    nsv5531243copy number variation1nstd206human GRCh38 chr16: 82,069,175-82,464,363 , GRCh37.p13 chr16: 82,102,780-82,497,968 HSD17B2, MPHOSPH6, 4 more genes
    nsv5517938copy number variation1nstd206human GRCh38 chr16: 82,149,966-82,195,985 , GRCh37.p13 chr16: 82,183,571-82,229,590 MPHOSPH6, RN7SKP190
    nsv5358438translocation1nstd200human GRCh38 chr16: 82,160,872-82,160,872 , GRCh38 chr16: 82,160,929-82,160,929 , GRCh37.p13 chr16: 82,194,477-82,194,477 , GRCh37.p13 chr16: 82,194,534-82,194,534 MPHOSPH6
    nsv5292893copy number variation1nstd204human GRCh38.p13 chr16: 82,138,301-82,146,500 , GRCh37.p13 chr16: 82,171,906-82,180,105 MPHOSPH6
    nsv5193541mobile element insertion1nstd203human GRCh38 chr16: 82,156,441-82,156,456 , GRCh37.p13 chr16: 82,190,046-82,190,061 MPHOSPH6
    nsv5149846mobile element insertion1nstd203human GRCh38 chr16: 82,165,114-82,165,145 , GRCh37.p13 chr16: 82,198,719-82,198,750 MPHOSPH6
    nsv5009718copy number variation1nstd200human GRCh38 chr16: 82,107,878-82,147,858 , GRCh37.p13 chr16: 82,141,483-82,181,463 MTCYBP28, MTND6P28, 1 more genes
    nsv4866918copy number variation1nstd200human GRCh37 chr16: 82,141,483-82,181,463 , GRCh38.p12 chr16: 82,107,878-82,147,858 MPHOSPH6, MTCYBP28, 1 more genes
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729840copy number variation1nstd102humanUncertain significance GRCh37 chr16: 82,019,507-82,180,338 , GRCh38.p12 chr16: 81,985,902-82,146,733 SDR42E1, LOC112268169, 5 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4684275copy number variation1nstd102humanUncertain significance GRCh37 chr16: 82,181,608-83,669,641 , GRCh38.p12 chr16: 82,148,003-83,636,036 RN7SL134P, LOC100419639, 9 more genes
    nsv4679797copy number variation1nstd189human GRCh37.p13 chr16: 82,180,760-83,621,025 , GRCh38.p12 chr16: 82,147,155-83,587,420 CDH13, MPHOSPH6, 9 more genes
    nsv4675465copy number variation1nstd102humanUncertain significance GRCh37 chr16: 81,982,623-82,831,574 , GRCh38.p12 chr16: 81,949,018-82,797,969 PLCG2, LOC100419639, 13 more genes
    nsv4675294copy number variation1nstd102humanUncertain significance GRCh37 chr16: 82,189,697-83,175,710 , GRCh38.p12 chr16: 82,156,092-83,142,105 RN7SKP190, RN7SL134P, 7 more genes
    nsv4675287copy number variation1nstd102humanLikely benign GRCh37 chr16: 81,983,037-83,067,299 , GRCh38.p12 chr16: 81,949,432-83,033,694 LOC112268169, RN7SL134P, 15 more genes
    nsv4675087copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 80,476,611-82,397,606 , GRCh38.p12 chr16: 80,442,714-82,364,001 GCSH, HSD17B2, 31 more genes
    nsv4622523copy number variation1nstd183human GRCh37 chr16: 82,179,757-83,670,446 , GRCh38.p12 chr16: 82,146,152-83,636,841 CDH13-AS1, RN7SL134P, 9 more genes
    nsv4576099mobile element insertion1nstd166human GRCh37.p13 chr16: 82,190,046-82,190,046 , GRCh38.p12 chr16: 82,156,441-82,156,441 MPHOSPH6
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