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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5928006copy number variation1nstd209human GRCh38 chr16: 3,305,029-3,322,631 , GRCh37.p13 chr16: 3,355,029-3,372,631 ZNF75A, TIGD7, 1 more genes
    nsv5559401sequence alteration1nstd206human GRCh38 chr16: 3,242,091-3,336,960 , GRCh37.p13 chr16: 3,292,091-3,386,960 MEFV, ZNF75A, 4 more genes
    nsv5527821copy number variation1nstd206human GRCh38 chr16: 3,299,464-3,299,618 , GRCh37.p13 chr16: 3,349,464-3,349,618 TIGD7, ZNF263
    nsv5521969copy number variation1nstd206human GRCh38 chr16: 3,293,873-3,298,973 , GRCh37.p13 chr16: 3,343,873-3,348,973 TIGD7, ZNF263
    nsv5521358copy number variation1nstd206human GRCh38 chr16: 3,208,003-3,350,991 , GRCh37.p13 chr16: 3,258,003-3,400,991 MEFV, ZNF75A, 6 more genes
    nsv5349425translocation1nstd200human GRCh38 chr16: 3,299,464-3,299,464 , GRCh38 chr16: 3,299,618-3,299,618 , GRCh37.p13 chr16: 3,349,464-3,349,464 , GRCh37.p13 chr16: 3,349,618-3,349,618 TIGD7, ZNF263
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5009365copy number variation1nstd200human GRCh38 chr16: 2,872,374-3,325,224 , GRCh37.p13 chr16: 2,922,375-3,375,224 , ZNF205, 55 more genes
    nsv5007999copy number variation1nstd200human GRCh38 chr16: 3,304,128-3,329,667 , GRCh37.p13 chr16: 3,354,128-3,379,667 RPL7L1P19, ZNF75A, 1 more genes
    nsv5007998copy number variation1nstd200human GRCh38 chr16: 3,297,474-3,303,868 , GRCh37.p13 chr16: 3,347,474-3,353,868 ZNF75A, TIGD7, 1 more genes
    nsv4866458copy number variation1nstd200human GRCh37 chr16: 3,354,128-3,379,667 , GRCh38.p12 chr16: 3,304,128-3,329,667 TIGD7, ZNF75A, 1 more genes
    nsv4866457copy number variation1nstd200human GRCh37 chr16: 3,349,464-3,349,618 , GRCh38.p12 chr16: 3,299,464-3,299,618 TIGD7, ZNF263
    nsv4854343copy number variation1nstd200human GRCh37 chr16: 2,922,375-3,375,224 , GRCh38.p12 chr16: 2,872,374-3,325,224 , RNU1-125P, 55 more genes
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4456418copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,112,024-3,738,078 , GRCh38.p12 chr16: 3,062,023-3,688,077 ZNF597, ZNF205-AS1, 55 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4349832copy number variation1nstd102humanPathogenic GRCh37 chr16: 109,978-4,316,797 , GRCh38.p12 chr16: 59,980-4,266,796 LINC00235, RNF151, 269 more genes
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