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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5711946mobile element insertion1nstd211human GRCh38 chr10: 89,828,615-89,828,615 , GRCh37.p13 chr10: 91,588,372-91,588,372 LINC00865, LOC105378424
    nsv5489929copy number variation1nstd206human GRCh38 chr10: 89,808,883-90,278,467 , GRCh37.p13 chr10: 91,568,640-92,038,224 SNRPD2P1, LINC00865, 6 more genes
    nsv5481956copy number variation1nstd206human GRCh38 chr10: 89,829,484-89,834,296 , GRCh37.p13 chr10: 91,589,241-91,594,053 LINC00865, LOC105378424
    nsv5394930mobile element insertion1nstd206human GRCh38 chr10: 89,828,615-89,828,666 , GRCh37.p13 chr10: 91,588,372-91,588,423 LOC105378424, LINC00865
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4986576copy number variation1nstd200human GRCh38 chr10: 89,829,484-89,834,296 , GRCh37.p13 chr10: 91,589,241-91,594,053 LOC105378424, LINC00865
    nsv4986575copy number variation1nstd200human GRCh38 chr10: 89,825,685-89,963,918 , GRCh37.p13 chr10: 91,585,442-91,723,675 LINC01375, MARK2P16, 3 more genes
    nsv4973877copy number variation1nstd200human GRCh38 chr10: 89,366,953-89,877,440 , GRCh37.p13 chr10: 91,126,710-91,637,197 SLC16A12-AS1, LINC00865, 14 more genes
    nsv4838966copy number variation1nstd200human GRCh37 chr10: 91,585,442-91,723,675 , GRCh38.p12 chr10: 89,825,685-89,963,918 LINC01375, LOC105378424, 3 more genes
    nsv4833445copy number variation1nstd200human GRCh37 chr10: 91,126,710-91,637,197 , GRCh38.p12 chr10: 89,366,953-89,877,440 SLC16A12, PANK1, 14 more genes
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4680566copy number variation1nstd189human GRCh38.p12 chr10: 89,807,205-90,276,397 , GRCh37.p13 chr10: 91,566,962-92,036,154 SNRPD2P1, LINC00865, 6 more genes
    nsv4615910copy number variation1nstd183human GRCh37 chr10: 91,526,717-91,691,548 , GRCh38.p12 chr10: 89,766,960-89,931,791 KIF20B, LINC00865, 5 more genes
    nsv4601586copy number variation1nstd183human GRCh37 chr10: 91,568,567-92,036,154 , GRCh38.p12 chr10: 89,808,810-90,276,397 SNRPD2P1, LINC00865, 6 more genes
    nsv4385169copy number variation2nstd173human GRCh37 chr10: 91,568,315-92,036,154 , GRCh38.p12 chr10: 89,808,558-90,276,397 SNRPD2P1, LINC00865, 6 more genes
    nsv4375196copy number variation1nstd173human GRCh37 chr10: 91,529,955-91,622,204 , GRCh38.p12 chr10: 89,770,198-89,862,447 MARK2P16, LINC00865, 4 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4182255copy number variation1nstd166human GRCh37.p13 chr10: 91,587,048-91,592,254 , GRCh38.p12 chr10: 89,827,291-89,832,497 LOC105378424, LINC00865
    nsv4180839copy number variation1nstd166human GRCh37.p13 chr10: 91,589,241-91,594,053 , GRCh38.p12 chr10: 89,829,484-89,834,296 LINC00865, LOC105378424
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