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Items: 1 to 20 of 617

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7064153inversion1nstd229human GRCh38 chr16: 463,012-758,884 , GRCh37.p13 chr16: 513,012-808,884 LINC00235, ANTKMT, 27 more genes
    nsv6973281copy number variation1nstd229human GRCh38 chr16: 622,106-656,922 , GRCh37.p13 chr16: 672,106-706,922 METTL26, LOC105371038, 6 more genes
    nsv6970011copy number variation1nstd229human GRCh38 chr16: 663,301-676,500 , GRCh37.p13 chr16: 713,301-726,500 WDR90, RHOT2, 1 more genes
    nsv6966485copy number variation1nstd229human GRCh38 chr16: 539,563-712,009 , GRCh37.p13 chr16: 589,563-762,009 RHBDL1, PIGQ, 18 more genes
    nsv6962817copy number variation1nstd229human GRCh38 chr16: 657,292-660,828 , GRCh37.p13 chr16: 707,292-710,828 WDR90
    nsv6961287copy number variation1nstd229human GRCh38 chr16: 659,987-664,845 , GRCh37.p13 chr16: 709,987-714,845 WDR90
    nsv6958605copy number variation1nstd229human GRCh38 chr16: 628,893-653,888 , GRCh37.p13 chr16: 678,893-703,888 METTL26, LOC105371038, 6 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
    nsv6515368copy number variation1nstd223human GRCh38 chr16: 622,106-656,924 , GRCh37.p13 chr16: 672,106-706,924 TRG-CCC2-2, METTL26, 6 more genes
    nsv6314105copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827 HBA2, LUC7L, 87 more genes
    nsv6273536copy number variation1nstd214human GRCh38 chr16: 659,490-659,548 , GRCh37.p13 chr16: 709,490-709,548 , WDR90
    nsv6202837copy number variation1nstd214human GRCh38 chr16: 665,256-665,309 , GRCh37.p13 chr16: 715,256-715,309 WDR90
    nsv6200435copy number variation1nstd214human GRCh38 chr16: 659,520-659,578 , GRCh37.p13 chr16: 709,520-709,578 , WDR90
    nsv6191826copy number variation1nstd214human GRCh38 chr16: 665,214-665,263 , GRCh37.p13 chr16: 715,214-715,263 WDR90
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
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