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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7061637inversion1nstd229human GRCh38 chr16: 67,211,127-67,211,191 , GRCh37.p13 chr16: 67,245,030-67,245,094 FBXL9P
    nsv6981504copy number variation1nstd229human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 ELMO3, MIR328, 1 more genes
    nsv6514406copy number variation1nstd223human GRCh38 chr16: 67,219,762-67,220,078 , GRCh37.p13 chr16: 67,253,665-67,253,981 FBXL9P
    nsv6508185copy number variation1nstd223human GRCh38 chr16: 67,223,232-67,224,705 , GRCh37.p13 chr16: 67,257,135-67,258,608 FBXL9P
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6120675copy number variation1nstd186human GRCh37 chr16: 67,253,676-67,253,981 , GRCh38.p12 chr16: 67,219,773-67,220,078 FBXL9P
    nsv6039247copy number variation1nstd212human GRCh38 chr16: 67,219,764-67,220,078 , GRCh37.p13 chr16: 67,253,667-67,253,981 FBXL9P
    nsv6023823copy number variation1nstd212human GRCh38 chr16: 67,202,558-67,205,520 , GRCh37.p13 chr16: 67,236,461-67,239,423 FBXL9P, ELMO3, 1 more genes
    nsv5943633copy number variation1nstd209human GRCh38 chr16: 67,219,762-67,220,077 , GRCh37.p13 chr16: 67,253,665-67,253,980 FBXL9P
    nsv5647040insertion1nstd207human GRCh38 chr16: 67,209,395-67,209,395 , GRCh37.p13 chr16: 67,243,298-67,243,298 FBXL9P
    nsv5600171copy number variation1nstd207human GRCh38 chr16: 67,219,762-67,220,077 , GRCh37.p13 chr16: 67,253,665-67,253,980 FBXL9P
    nsv5533342copy number variation1nstd206human GRCh38 chr16: 67,218,892-67,219,587 , GRCh37.p13 chr16: 67,252,795-67,253,490 FBXL9P
    nsv5532090copy number variation1nstd206human GRCh38 chr16: 67,223,660-67,225,381 , GRCh37.p13 chr16: 67,257,563-67,259,284 FBXL9P, TMEM208
    nsv5520293copy number variation1nstd206human GRCh38 chr16: 67,219,773-67,220,078 , GRCh37.p13 chr16: 67,253,676-67,253,981 FBXL9P
    nsv5383052mobile element deletion2nstd186human GRCh37 chr16: 67,253,676-67,253,981 , GRCh38.p12 chr16: 67,219,773-67,220,078 FBXL9P
    nsv5271417copy number variation1nstd204human GRCh38.p13 chr16: 67,219,801-67,220,100 , GRCh37.p13 chr16: 67,253,704-67,254,003 FBXL9P
    nsv5211384mobile element deletion1nstd204human GRCh38.p13 chr16: 67,219,773-67,220,078 , GRCh37.p13 chr16: 67,253,676-67,253,981 FBXL9P
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