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Items: 1 to 20 of 496

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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
    nsv6977619copy number variation1nstd229human GRCh38 chr16: 677,793-687,365 , GRCh37.p13 chr16: 727,793-737,365 STUB1-DT, STUB1, 3 more genes
    nsv6968026copy number variation1nstd229human GRCh38 chr16: 686,022-686,719 , GRCh37.p13 chr16: 736,022-736,719 WDR24
    nsv6966485copy number variation1nstd229human GRCh38 chr16: 539,563-712,009 , GRCh37.p13 chr16: 589,563-762,009 RHBDL1, PIGQ, 18 more genes
    nsv6964587copy number variation1nstd229human GRCh38 chr16: 681,201-683,000 , GRCh37.p13 chr16: 731,201-733,000 STUB1, JMJD8, 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
    nsv6637644copy number variation1nstd102humanUncertain significance GRCh37 chr16: 726,789-1,066,511 , GRCh38.p12 chr16: 676,789-1,016,511 WDR24, STUB1, 21 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
    nsv6314105copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827 HBA2, LUC7L, 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
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5279314copy number variation1nstd204human GRCh38.p13 chr16: 631,501-737,100 , GRCh37.p13 chr16: 681,501-787,100 , CIAO3, 18 more genes
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5263615copy number variation1nstd204human GRCh38.p13 chr16: 504,601-857,400 , GRCh37.p13 chr16: 554,601-907,400 , LINC00235, 36 more genes
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