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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,293,141-5,971,108 , GRCh38.p12 chr16: 3,243,141-5,921,107 MGRN1, CORO7, 76 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
    nsv6977592copy number variation1nstd229human GRCh38 chr16: 3,246,328-3,262,674 , GRCh37.p13 chr16: 3,296,328-3,312,674 LINC00921, MEFV
    nsv6974280copy number variation1nstd229human GRCh38 chr16: 3,125,283-3,274,634 , GRCh37.p13 chr16: 3,175,284-3,324,634 TRK-CTT4-1, ZNF200, 23 more genes
    nsv6968778copy number variation1nstd229human GRCh38 chr16: 3,206,227-3,444,939 , GRCh37.p13 chr16: 3,256,227-3,494,939 MEFV, ZNF597, 18 more genes
    nsv6968134copy number variation1nstd229human GRCh38 chr16: 3,257,601-3,262,400 , GRCh37.p13 chr16: 3,307,601-3,312,400 LINC00921
    nsv6968061copy number variation1nstd229human GRCh38 chr16: 3,174,701-3,284,700 , GRCh37.p13 chr16: 3,224,702-3,334,700 MEFV, TRP-TGG3-5, 14 more genes
    nsv6966465copy number variation1nstd229human GRCh38 chr16: 3,206,167-3,270,350 , GRCh37.p13 chr16: 3,256,167-3,320,350 OR1F2P, MEFV, 3 more genes
    nsv6961514copy number variation1nstd229human GRCh38 chr16: 3,267,155-3,288,170 , GRCh37.p13 chr16: 3,317,155-3,338,170 LINC00921, ZNF263
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6509422copy number variation1nstd223human GRCh38 chr16: 3,161,768-3,335,002 , GRCh37.p13 chr16: 3,211,769-3,385,002 TRP-TGG4-1, LINC00921, 19 more genes
    nsv6505153copy number variation1nstd223human GRCh38 chr16: 3,265,350-3,269,934 , GRCh37.p13 chr16: 3,315,350-3,319,934 LINC00921
    nsv6502951copy number variation1nstd223human GRCh38 chr16: 3,260,983-3,266,388 , GRCh37.p13 chr16: 3,310,983-3,316,388 LINC00921
    nsv6498301copy number variation1nstd223human GRCh38 chr16: 3,260,452-3,263,575 , GRCh37.p13 chr16: 3,310,452-3,313,575 LINC00921
    nsv6497789copy number variation1nstd223human GRCh38 chr16: 3,261,413-3,267,927 , GRCh37.p13 chr16: 3,311,413-3,317,927 LINC00921
    nsv6310074copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,293,141-3,929,917 , GRCh38.p12 chr16: 3,243,141-3,879,916 MTRNR2L4, TRAP1, 26 more genes
    nsv6290044copy number variation1nstd218human GRCh38.p12 chr16: 2,757,479-3,781,321 , GRCh37 chr16: 2,807,480-3,831,322 , CREBBP, 87 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133274copy number variation1nstd213human GRCh37 chr16: 2,660,000-3,710,001 , GRCh38.p12 chr16: 2,609,999-3,660,000 DNASE1, MEFV, 90 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
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