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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5469419copy number variation1nstd206human GRCh38 chr5: 56,906,618-56,907,884 , GRCh37.p13 chr5: 56,202,445-56,203,711 SETD9
    nsv5317919copy number variation1nstd204human GRCh38.p13 chr5: 56,908,237-56,927,642 , GRCh37.p13 chr5: 56,204,064-56,223,469 SETD9, MIER3
    nsv5316823copy number variation1nstd204human GRCh38.p13 chr5: 56,739,373-56,917,641 , GRCh37.p13 chr5: 56,035,200-56,213,468 LOC105378979, MAP3K1, 3 more genes
    nsv5237910copy number variation1nstd204human GRCh38.p13 chr5: 56,908,301-56,926,800 , GRCh37.p13 chr5: 56,204,128-56,222,627 SETD9, MIER3
    nsv5232917copy number variation1nstd204human GRCh38.p13 chr5: 56,899,336-56,922,049 , GRCh37.p13 chr5: 56,195,163-56,217,876 MIER3, LOC105378980, 1 more genes
    nsv5230116copy number variation1nstd204human GRCh38.p13 chr5: 56,908,230-56,928,324 , GRCh37.p13 chr5: 56,204,057-56,224,151 SETD9, MIER3
    nsv5228124copy number variation1nstd204human GRCh38.p13 chr5: 56,923,050-56,924,249 , GRCh37.p13 chr5: 56,218,877-56,220,076 SETD9, MIER3
    nsv5225519copy number variation1nstd204human GRCh38.p13 chr5: 56,912,555-56,914,619 , GRCh37.p13 chr5: 56,208,382-56,210,446 SETD9
    nsv5222208copy number variation1nstd204human GRCh38.p13 chr5: 56,738,401-56,917,600 , GRCh37.p13 chr5: 56,034,228-56,213,427 LOC105378980, MAP3K1, 2 more genes
    nsv4948774copy number variation1nstd200human GRCh38 chr5: 56,908,242-56,927,639 , GRCh37.p13 chr5: 56,204,069-56,223,466 MIER3, SETD9
    nsv4805529copy number variation1nstd200human GRCh37 chr5: 56,204,069-56,223,466 , GRCh38.p12 chr5: 56,908,242-56,927,639 MIER3, SETD9
    nsv4728887copy number variation1nstd102humanUncertain significance GRCh37 chr5: 55,867,380-56,217,595 , GRCh38.p12 chr5: 56,571,553-56,921,768 LOC105378980, C5orf67, 4 more genes
    nsv4598170copy number variation1nstd183human GRCh37 chr5: 56,212,810-56,215,776 , GRCh38.p12 chr5: 56,916,983-56,919,949 SETD9, MIER3
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4131013copy number variation1nstd166human GRCh37.p13 chr5: 56,204,054-56,223,495 , GRCh38.p12 chr5: 56,908,227-56,927,668 MIER3, SETD9
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3917914copy number variation1nstd102humanUncertain significance NCBI36 chr5: 56,048,895-56,361,116 , GRCh37 chr5: 56,013,138-56,325,359 , GRCh38 chr5: 56,717,311-57,029,532 MAP3K1, LOC105378980, 4 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
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