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Items: 1 to 20 of 202

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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
    nsv5912545copy number variation1nstd209human GRCh38 chr10: 122,260,973-122,273,514 , GRCh37.p13 chr10: 124,020,488-124,033,029 BTBD16
    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
    nsv5354534translocation1nstd200human GRCh38 chr10: 122,302,499-122,302,499 , GRCh38 chr10: 122,302,269-122,302,269 , GRCh37.p13 chr10: 124,061,784-124,061,784 , GRCh37.p13 chr10: 124,062,014-124,062,014 BTBD16
    nsv5304664copy number variation1nstd204human GRCh38.p13 chr10: 122,302,259-122,302,508 , GRCh37.p13 chr10: 124,061,774-124,062,023 BTBD16
    nsv4983950copy number variation1nstd200human GRCh38 chr10: 122,260,725-122,285,269 , GRCh37.p13 chr10: 124,020,240-124,044,784 BTBD16
    nsv4977302copy number variation1nstd200human GRCh38 chr10: 122,316,583-122,332,337 , GRCh37.p13 chr10: 124,076,098-124,091,852 BTBD16
    nsv4977301copy number variation1nstd200human GRCh38 chr10: 122,312,210-122,316,849 , GRCh37.p13 chr10: 124,071,725-124,076,364 BTBD16
    nsv4845766copy number variation1nstd200human GRCh37 chr10: 124,052,624-124,052,972 , GRCh38.p12 chr10: 122,293,109-122,293,457 BTBD16
    nsv4840326copy number variation1nstd200human GRCh37 chr10: 124,076,098-124,091,852 , GRCh38.p12 chr10: 122,316,583-122,332,337 BTBD16
    nsv4838470copy number variation1nstd200human GRCh37 chr10: 124,071,725-124,076,364 , GRCh38.p12 chr10: 122,312,210-122,316,849 BTBD16
    nsv4832588copy number variation1nstd200human GRCh37 chr10: 124,020,486-124,033,030 , GRCh38.p12 chr10: 122,260,971-122,273,515 BTBD16
    nsv4680441copy number variation1nstd189human GRCh37.p13 chr10: 123,927,244-124,112,168 , GRCh38.p12 chr10: 122,167,729-122,352,653 TACC2, BTBD16, 1 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
    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
    nsv4370830copy number variation1nstd173human GRCh37 chr10: 124,077,860-124,107,484 , GRCh38.p12 chr10: 122,318,345-122,347,969 RNU6-728P, BTBD16
    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
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