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Items: 1 to 20 of 155

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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
    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
    nsv5512526copy number variation1nstd206human GRCh38 chr10: 122,878,779-122,878,865 , GRCh37.p13 chr10: 124,638,295-124,638,381 FAM24B, C10orf88B, 1 more genes
    nsv5500267copy number variation1nstd206human GRCh38 chr10: 122,863,033-122,904,137 , GRCh37.p13 chr10: 124,622,549-124,663,653 FAM24B, C10orf88B, 1 more genes
    nsv4729290copy number variation1nstd102humanUncertain significance GRCh37 chr10: 124,488,148-124,607,872 , GRCh38.p12 chr10: 122,728,632-122,848,356 DMBT1L1, FAM24B-CUZD1, 2 more genes
    nsv4728778copy number variation1nstd102humanUncertain significance GRCh37 chr10: 124,439,521-124,607,872 , GRCh38.p12 chr10: 122,680,005-122,848,356 CUZD1, FAM24B, 3 more genes
    nsv4679699copy number variation1nstd189human GRCh37.p13 chr10: 124,478,359-125,318,025 , GRCh38.p12 chr10: 122,718,843-123,558,509 ACADSB, HMX2, 15 more genes
    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
    nsv4481390mobile element insertion1nstd166human GRCh37.p13 chr10: 124,616,811-124,616,811 , GRCh38.p12 chr10: 122,857,295-122,857,295 FAM24B-CUZD1, FAM24B
    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
    nsv4205050copy number variation1nstd166human GRCh37.p13 chr10: 124,638,295-124,638,381 , GRCh38.p12 chr10: 122,878,779-122,878,865 FAM24B, C10orf88B, 1 more genes
    nsv4204742copy number variation1nstd166human GRCh37.p13 chr10: 124,627,760-124,627,954 , GRCh38.p12 chr10: 122,868,244-122,868,438 FAM24B-CUZD1, FAM24B
    nsv4196121copy number variation1nstd166human GRCh37.p13 chr10: 124,492,192-124,610,364 , GRCh38.p12 chr10: 122,732,676-122,850,848 DMBT1L1, CUZD1, 2 more genes
    nsv3969474insertion1nstd168human GRCh38 chr10: 122,836,561-122,851,174 , GRCh37.p13 chr10: 124,596,077-124,610,690 CUZD1, FAM24B, 1 more genes
    nsv3968882copy number variation1nstd168human GRCh38 chr10: 122,824,587-122,840,072 , GRCh37.p13 chr10: 124,584,103-124,599,588 CUZD1, FAM24B-CUZD1
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