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Items: 1 to 20 of 460

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977326inversion1nstd209human GRCh38 chr5: 176,286,704-177,635,736 , GRCh37.p13 chr5: 175,713,707-177,062,737 , CLTB, 46 more genes
    nsv5966551insertion1nstd209human GRCh38 chr5: 177,000,498-177,000,498 , GRCh37.p13 chr5: 176,427,499-176,427,499 UIMC1
    nsv5905631copy number variation1nstd209human GRCh38 chr5: 176,979,625-176,979,758 , GRCh37.p13 chr5: 176,406,626-176,406,759 UIMC1
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5894661copy number variation1nstd209human GRCh38 chr5: 176,919,460-176,919,562 , GRCh37.p13 chr5: 176,346,461-176,346,563 UIMC1
    nsv5890062copy number variation1nstd209human GRCh38 chr5: 176,061,658-178,007,127 , GRCh37.p13 chr5: 175,488,661-177,434,128 , DBN1, 65 more genes
    nsv5888029copy number variation1nstd209human GRCh38 chr5: 176,995,540-176,998,465 , GRCh37.p13 chr5: 176,422,541-176,425,466 UIMC1
    nsv5842481copy number variation1nstd209human GRCh38 chr5: 176,995,523-176,997,372 , GRCh37.p13 chr5: 176,422,524-176,424,373 UIMC1
    nsv5678728mobile element insertion1nstd211human GRCh38 chr5: 176,920,489-176,920,489 , GRCh37.p13 chr5: 176,347,490-176,347,490 UIMC1
    nsv5633976insertion1nstd207human GRCh38 chr5: 176,962,494-176,962,494 , GRCh37.p13 chr5: 176,389,495-176,389,495 UIMC1
    nsv5625805insertion1nstd207human GRCh38 chr5: 176,962,135-176,962,135 , GRCh37.p13 chr5: 176,389,136-176,389,136 UIMC1
    nsv5574795copy number variation1nstd207human GRCh38 chr5: 176,960,578-176,963,178 , GRCh37.p13 chr5: 176,387,579-176,390,179 UIMC1
    nsv5569185copy number variation1nstd207human GRCh38 chr5: 176,984,239-176,984,314 , GRCh37.p13 chr5: 176,411,240-176,411,315 UIMC1
    nsv5565037copy number variation1nstd207human GRCh38 chr5: 177,011,077-177,012,578 , GRCh37.p13 chr5: 176,438,078-176,439,579 UIMC1
    nsv5471906copy number variation1nstd206human GRCh38 chr5: 176,989,588-176,990,690 , GRCh37.p13 chr5: 176,416,589-176,417,691 UIMC1
    nsv5469888copy number variation1nstd206human GRCh38 chr5: 176,986,982-176,998,295 , GRCh37.p13 chr5: 176,413,983-176,425,296 UIMC1
    nsv5466061copy number variation1nstd206human GRCh38 chr5: 177,011,065-177,012,592 , GRCh37.p13 chr5: 176,438,066-176,439,593 UIMC1
    nsv5462079copy number variation1nstd206human GRCh38 chr5: 176,960,586-176,963,179 , GRCh37.p13 chr5: 176,387,587-176,390,180 UIMC1
    nsv5456741copy number variation1nstd206human GRCh38 chr5: 177,021,924-177,069,675 , GRCh37.p13 chr5: 176,448,925-176,496,676 ZNF346, UIMC1
    nsv5456464copy number variation1nstd206human GRCh38 chr5: 176,990,105-176,991,870 , GRCh37.p13 chr5: 176,417,106-176,418,871 UIMC1
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