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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138410copy number variation1nstd232human GRCh37.p13 chr16: 1,305,054-1,305,119 , GRCh38.p12 chr16: 1,255,053-1,255,118 TPSD1
    nsv7098880copy number variation1nstd102humanPathogenic GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378 TPSP1, NPW, 78 more genes
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7094663copy number variation2nstd102humanPathogenic GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266 TPSP2, PRR25, 83 more genes
    nsv7073654inversion1nstd229human GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907 UBE2I, CRAMP1, 45 more genes
    nsv7067435inversion1nstd229human GRCh38 chr16: 1,244,682-1,277,895 , GRCh37.p13 chr16: 1,294,683-1,327,896 TPSD1, PRSS29P, 1 more genes
    nsv6977134copy number variation1nstd229human GRCh38 chr16: 951,401-1,472,200 , GRCh37.p13 chr16: 1,001,401-1,522,201 TPSG1, TPSAB1, 27 more genes
    nsv6976857copy number variation1nstd229human GRCh38 chr16: 1,259,501-1,303,500 , GRCh37.p13 chr16: 1,309,502-1,353,501 TPSP2, PRSS29P, 2 more genes
    nsv6976078copy number variation1nstd229human GRCh38 chr16: 1,259,470-1,303,485 , GRCh37.p13 chr16: 1,309,471-1,353,486 TPSD1, TPSP2, 2 more genes
    nsv6975915copy number variation1nstd229human GRCh38 chr16: 1,198,320-1,301,006 , GRCh37.p13 chr16: 1,248,320-1,351,007 TPSAB1, CACNA1H, 6 more genes
    nsv6969363copy number variation1nstd229human GRCh38 chr16: 1,231,537-1,395,440 , GRCh37.p13 chr16: 1,281,538-1,445,441 PRSS29P, RPS20P2, 10 more genes
    nsv6962303copy number variation1nstd229human GRCh38 chr16: 1,118,142-1,673,202 , GRCh37.p13 chr16: 1,168,142-1,723,203 TJP1P1, TELO2, 27 more genes
    nsv6959750copy number variation1nstd229human GRCh38 chr16: 1,245,046-1,261,321 , GRCh37.p13 chr16: 1,295,047-1,311,322 TPSD1, PRSS29P
    nsv6959275copy number variation1nstd229human GRCh38 chr16: 1,259,070-1,261,756 , GRCh37.p13 chr16: 1,309,071-1,311,757 PRSS29P, TPSD1
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 more genes
    nsv6637768copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054 CRAMP1, LOC105371046, 57 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6510722copy number variation1nstd223human GRCh38 chr16: 1,226,521-1,428,295 , GRCh37.p13 chr16: 1,276,521-1,478,296 TPSB2, TPSP1, 15 more genes
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