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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7095050copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,050,104-84,050,912 , GRCh38.p12 chr16: 84,016,499-84,017,307 SLC38A8
    nsv7094697copy number variation1nstd102humanUncertain significance GRCh37 chr16: 84,043,389-84,043,502 , GRCh38.p12 chr16: 84,009,784-84,009,897 SLC38A8
    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
    nsv7076578inversion1nstd229human GRCh38 chr16: 83,742,713-84,033,267 , GRCh37.p13 chr16: 83,776,318-84,066,872 HSBP1, NECAB2, 6 more genes
    nsv7076150inversion1nstd229human GRCh38 chr16: 83,426,720-84,571,834 , GRCh37.p13 chr16: 83,460,325-84,605,440 , LOC648774, 23 more genes
    nsv7073806inversion1nstd229human GRCh38 chr16: 83,959,188-84,022,126 , GRCh37.p13 chr16: 83,992,793-84,055,731 SLC38A8, OSGIN1, 1 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
    nsv7058832inversion1nstd229human GRCh38 chr16: 84,010,348-84,010,523 , GRCh37.p13 chr16: 84,043,953-84,044,128 SLC38A8
    nsv6997112copy number variation1nstd229human GRCh38 chr16: 84,023,743-84,024,617 , GRCh37.p13 chr16: 84,057,348-84,058,222 SLC38A8
    nsv6996878copy number variation1nstd229human GRCh38 chr16: 84,014,346-84,016,339 , GRCh37.p13 chr16: 84,047,951-84,049,944 SLC38A8
    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
    nsv6995842copy number variation1nstd229human GRCh38 chr16: 84,014,452-84,019,003 , GRCh37.p13 chr16: 84,048,057-84,052,608 SLC38A8
    nsv6995142copy number variation1nstd229human GRCh38 chr16: 83,870,301-84,028,700 , GRCh37.p13 chr16: 83,903,906-84,062,305 SLC38A8, MLYCD, 3 more genes
    nsv6994680copy number variation1nstd229human GRCh38 chr16: 84,019,029-84,025,305 , GRCh37.p13 chr16: 84,052,634-84,058,910 SLC38A8
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993903copy number variation1nstd229human GRCh38 chr16: 83,896,130-84,027,702 , GRCh37.p13 chr16: 83,929,735-84,061,307 MLYCD, NECAB2, 3 more genes
    nsv6993775copy number variation1nstd229human GRCh38 chr16: 84,015,001-84,021,800 , GRCh37.p13 chr16: 84,048,606-84,055,405 SLC38A8
    nsv6993757copy number variation1nstd229human GRCh38 chr16: 84,006,001-84,008,500 , GRCh37.p13 chr16: 84,039,606-84,042,105 SLC38A8
    nsv6992668copy number variation1nstd229human GRCh38 chr16: 83,866,843-84,024,110 , GRCh37.p13 chr16: 83,900,448-84,057,715 SLC38A8, MLYCD, 3 more genes
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