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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5925709copy number variation1nstd209human GRCh38 chr10: 121,964,397-121,964,690 , GRCh37.p13 chr10: 123,723,912-123,724,205 NSMCE4A
    nsv5695798mobile element insertion1nstd211human GRCh38 chr10: 121,969,487-121,969,487 , GRCh37.p13 chr10: 123,729,002-123,729,002 NSMCE4A
    nsv5672603copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 119,302,758-124,813,305 , GRCh38.p12 chr10: 117,543,247-123,053,789 ACADSB, DMBT1, 84 more genes
    nsv5510896copy number variation1nstd206human GRCh38 chr10: 121,962,193-121,963,707 , GRCh37.p13 chr10: 123,721,708-123,723,222 NSMCE4A
    nsv5495562copy number variation1nstd206human GRCh38 chr10: 121,954,605-121,957,689 , GRCh37.p13 chr10: 123,714,120-123,717,204 NSMCE4A
    nsv5133034mobile element insertion1nstd203human GRCh38 chr10: 121,957,187-121,957,202 , GRCh37.p13 chr10: 123,716,702-123,716,717 NSMCE4A
    nsv5130011mobile element insertion1nstd203human GRCh38 chr10: 121,969,015-121,969,030 , GRCh37.p13 chr10: 123,728,530-123,728,545 NSMCE4A
    nsv4977287copy number variation1nstd200human GRCh38 chr10: 121,962,373-121,963,991 , GRCh37.p13 chr10: 123,721,888-123,723,506 NSMCE4A
    nsv4848259copy number variation1nstd200human GRCh37 chr10: 123,721,888-123,723,506 , GRCh38.p12 chr10: 121,962,373-121,963,991 NSMCE4A
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4675857copy number variation1nstd102humanUncertain significance GRCh37 chr10: 123,232,922-124,638,514 , GRCh38.p12 chr10: 121,473,408-122,878,998 LOC105378525, HTRA1, 20 more genes
    nsv4614149copy number variation1nstd183human GRCh37 chr10: 123,543,592-123,813,690 , GRCh38.p12 chr10: 121,784,077-122,054,175 NSMCE4A, ATE1, 2 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4349508copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,024,753-124,942,806 , GRCh38.p12 chr10: 115,265,276-123,183,290 PRLHR, LOC105378513, 121 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4208989copy number variation1nstd166human GRCh37.p13 chr10: 123,721,898-126,209,916 , GRCh38.p12 chr10: 121,962,383-124,521,347 , CHST15, 44 more genes
    nsv3924720copy number variation1nstd102humanPathogenic GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133 OR6L2P, RPL19P16, 208 more genes
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
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