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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141429copy number variation1nstd232human GRCh37.p13 chr16: 1,358,387-1,358,438 , GRCh38.p12 chr16: 1,308,386-1,308,437 UBE2I
    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
    nsv7064563inversion1nstd229human GRCh38 chr16: 1,279,128-1,693,078 , GRCh37.p13 chr16: 1,329,129-1,743,079 UNKL, CRAMP1, 20 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
    nsv6972844copy number variation1nstd229human GRCh38 chr16: 1,323,764-1,324,331 , GRCh37.p13 chr16: 1,373,765-1,374,332 UBE2I
    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
    nsv6968853copy number variation1nstd229human GRCh38 chr16: 1,304,546-1,308,968 , GRCh37.p13 chr16: 1,354,547-1,358,969 UBE2I
    nsv6968644copy number variation1nstd229human GRCh38 chr16: 1,319,632-1,358,036 , GRCh37.p13 chr16: 1,369,633-1,408,037 TSR3, UBE2I, 3 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
    nsv6961031copy number variation1nstd229human GRCh38 chr16: 1,316,401-1,318,500 , GRCh37.p13 chr16: 1,366,402-1,368,501 UBE2I
    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
    nsv6623402copy number variation1nstd224human GRCh37 chr16: 1,371,154-1,421,606 , GRCh38.p12 chr16: 1,321,153-1,371,605 UBE2I, BAIAP3, 5 more genes
    nsv6578605inversion1nstd223human GRCh38 chr16: 1,320,729-1,325,414 , GRCh37.p13 chr16: 1,370,730-1,375,415 UBE2I
    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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