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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095036copy number variation1nstd102humanPathogenic GRCh37 chr16: 622,268-632,290 , GRCh38.p12 chr16: 572,268-582,290 PIGQ
    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
    nsv7094577copy number variation1nstd102humanUncertain significance GRCh37 chr16: 289,853-626,274 , GRCh38.p12 chr16: 239,854-576,274 ARHGDIG, DECR2, 17 more genes
    nsv7094575copy number variation1nstd102humanPathogenic GRCh37 chr16: 256,302-633,035 , GRCh38.p12 chr16: 206,303-583,035 FAM234A, RPL23AP5, 19 more genes
    nsv7064153inversion1nstd229human GRCh38 chr16: 463,012-758,884 , GRCh37.p13 chr16: 513,012-808,884 LINC00235, ANTKMT, 27 more genes
    nsv6977185copy number variation1nstd229human GRCh38 chr16: 573,163-586,883 , GRCh37.p13 chr16: 623,163-636,883 PIGQ
    nsv6974857copy number variation1nstd229human GRCh38 chr16: 394,003-596,867 , GRCh37.p13 chr16: 444,003-646,867 CAPN15, MIR5587, 9 more genes
    nsv6974504copy number variation1nstd229human GRCh38 chr16: 581,493-589,241 , GRCh37.p13 chr16: 631,493-639,241 PIGQ, RAB40C
    nsv6973009copy number variation1nstd229human GRCh38 chr16: 584,489-589,099 , GRCh37.p13 chr16: 634,489-639,099 RAB40C, PIGQ
    nsv6970436copy number variation1nstd229human GRCh38 chr16: 528,697-616,825 , GRCh37.p13 chr16: 578,697-666,825 RAB40C, MIR5587, 5 more genes
    nsv6968646copy number variation1nstd229human GRCh38 chr16: 547,723-584,316 , GRCh37.p13 chr16: 597,723-634,316 CAPN15, NHLRC4, 2 more genes
    nsv6966485copy number variation1nstd229human GRCh38 chr16: 539,563-712,009 , GRCh37.p13 chr16: 589,563-762,009 RHBDL1, PIGQ, 18 more genes
    nsv6964525copy number variation1nstd229human GRCh38 chr16: 581,517-589,519 , GRCh37.p13 chr16: 631,517-639,519 PIGQ, RAB40C
    nsv6964018copy number variation1nstd229human GRCh38 chr16: 563,415-574,350 , GRCh37.p13 chr16: 613,415-624,350 PRR35, PIGQ, 1 more genes
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 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
    nsv6623477copy number variation1nstd224human GRCh37 chr16: 633,125-683,399 , GRCh38.p12 chr16: 583,125-633,399 RAB40C, METTL26, 2 more genes
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