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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142372insertion1nstd232human GRCh37.p13 chr16: 84,094,419-84,094,419 , GRCh38.p12 chr16: 84,060,814-84,060,814 MBTPS1
    nsv7095104copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,046,586-84,126,922 , GRCh38.p12 chr16: 84,012,981-84,093,317 MBTPS1, SLC38A8, 1 more genes
    nsv7094603copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,932,750-84,211,465 , GRCh38.p12 chr16: 83,899,145-84,177,859 NECAB2, HSDL1, 9 more genes
    nsv7076150inversion1nstd229human GRCh38 chr16: 83,426,720-84,571,834 , GRCh37.p13 chr16: 83,460,325-84,605,440 , LOC648774, 23 more genes
    nsv7069513inversion1nstd229human GRCh38 chr16: 83,832,179-84,528,985 , GRCh37.p13 chr16: 83,865,784-84,562,591 HSDL1, ATP2C2-AS1, 17 more genes
    nsv7060561inversion1nstd229human GRCh38 chr16: 84,098,869-84,513,647 , GRCh37.p13 chr16: 84,132,474-84,547,253 ADAD2, TAF1C, 11 more genes
    nsv6996402copy number variation1nstd229human GRCh38 chr16: 84,010,943-84,093,762 , GRCh37.p13 chr16: 84,044,548-84,127,367 MBTPS1, SLC38A8, 1 more genes
    nsv6995307copy number variation1nstd229human GRCh38 chr16: 84,084,301-84,092,100 , GRCh37.p13 chr16: 84,117,906-84,125,705 MBTPS1
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6989652copy number variation1nstd229human GRCh38 chr16: 83,870,081-84,053,349 , GRCh37.p13 chr16: 83,903,686-84,086,954 OSGIN1, NECAB2, 5 more genes
    nsv6988299copy number variation1nstd229human GRCh38 chr16: 84,079,767-84,084,643 , GRCh37.p13 chr16: 84,113,372-84,118,248 MBTPS1
    nsv6987544copy number variation1nstd229human GRCh38 chr16: 84,097,671-84,149,670 , GRCh37.p13 chr16: 84,131,276-84,183,275 LOC648774, DNAAF1, 2 more genes
    nsv6986001copy number variation1nstd229human GRCh38 chr16: 84,044,957-84,097,966 , GRCh37.p13 chr16: 84,078,562-84,131,571 MBTPS1
    nsv6985823copy number variation1nstd229human GRCh38 chr16: 84,029,193-84,083,254 , GRCh37.p13 chr16: 84,062,798-84,116,859 SLC38A8, RNA5SP432, 1 more genes
    nsv6984996copy number variation1nstd229human GRCh38 chr16: 84,041,109-84,055,125 , GRCh37.p13 chr16: 84,074,714-84,088,730 SLC38A8, MBTPS1
    nsv6984101copy number variation1nstd229human GRCh38 chr16: 84,000,751-84,060,549 , GRCh37.p13 chr16: 84,034,356-84,094,154 RNA5SP432, SLC38A8, 2 more genes
    nsv6981903copy number variation1nstd229human GRCh38 chr16: 83,878,443-84,573,896 , GRCh37.p13 chr16: 83,912,048-84,607,502 KCNG4, ATP2C2-AS1, 18 more genes
    nsv6978894copy number variation1nstd229human GRCh38 chr16: 84,114,620-84,339,946 , GRCh37.p13 chr16: 84,148,225-84,373,552 TAF1C, LOC648774, 8 more genes
    nsv6978872copy number variation1nstd229human GRCh38 chr16: 84,061,607-84,399,744 , GRCh37.p13 chr16: 84,095,212-84,433,350 WFDC1, MBTPS1, 9 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
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