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Items: 1 to 20 of 389

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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
    nsv5946262copy number variation1nstd209human GRCh38 chr16: 1,357,697-1,359,039 , GRCh37.p13 chr16: 1,407,698-1,409,040 GNPTG
    nsv5877203copy number variation1nstd209human GRCh38 chr16: 1,357,667-1,359,066 , GRCh37.p13 chr16: 1,407,668-1,409,067 GNPTG
    nsv5525470copy number variation1nstd206human GRCh38 chr16: 1,356,768-1,364,915 , GRCh37.p13 chr16: 1,406,769-1,414,916 UNKL, GNPTG
    nsv5522738copy number variation1nstd206human GRCh38 chr16: 1,356,879-1,357,113 , GRCh37.p13 chr16: 1,406,880-1,407,114 GNPTG
    nsv5515499copy number variation1nstd206human GRCh38 chr16: 1,357,677-1,359,077 , GRCh37.p13 chr16: 1,407,678-1,409,078 GNPTG
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5338882translocation1nstd200human GRCh37 chr16: 1,407,749-1,407,749 , GRCh37 chr16: 1,409,035-1,409,035 , GRCh38.p12 chr16: 1,357,748-1,357,748 , GRCh38.p12 chr16: 1,359,034-1,359,034 GNPTG
    nsv5305763copy number variation1nstd204human GRCh37.p13 chr16: 1,406,742-1,414,937 , GRCh38.p13 chr16: 1,356,741-1,364,936 UNKL, GNPTG
    nsv5301099copy number variation1nstd204human GRCh38.p13 chr16: 1,357,716-1,359,064 , GRCh37.p13 chr16: 1,407,717-1,409,065 GNPTG
    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
    nsv5264656copy number variation1nstd204human GRCh38.p13 chr16: 1,356,737-1,364,875 , GRCh37.p13 chr16: 1,406,738-1,414,876 GNPTG, UNKL
    nsv5263284copy number variation1nstd204human GRCh38.p13 chr16: 1,357,667-1,359,066 , GRCh37.p13 chr16: 1,407,668-1,409,067 GNPTG
    nsv5007874copy number variation1nstd200human GRCh38 chr16: 1,319,632-1,358,034 , GRCh37.p13 chr16: 1,369,633-1,408,035 RPS20P2, TSR3, 3 more genes
    nsv5002926copy number variation1nstd200human GRCh38 chr16: 1,356,768-1,364,915 , GRCh37.p13 chr16: 1,406,769-1,414,916 GNPTG, UNKL
    nsv5002925copy number variation1nstd200human GRCh38 chr16: 1,353,555-1,354,304 , GRCh37.p13 chr16: 1,403,556-1,404,305 GNPTG
    nsv4866354copy number variation1nstd200human GRCh37 chr16: 1,406,769-1,414,916 , GRCh38.p12 chr16: 1,356,768-1,364,915 UNKL, GNPTG
    nsv4729673copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,233,996-1,509,217 , GRCh38.p12 chr16: 1,183,996-1,459,216 LOC105371044, TPSB2, 19 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
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