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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7046164inversion1nstd229human GRCh38 chr5: 36,152,155-36,160,427 , GRCh37.p13 chr5: 36,152,257-36,160,529 LMBRD2, SKP2, 1 more genes
    nsv6777831copy number variation1nstd229human GRCh38 chr5: 36,135,619-36,143,017 , GRCh37.p13 chr5: 36,135,721-36,143,119 LMBRD2
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6762390copy number variation1nstd229human GRCh38 chr5: 36,115,047-36,119,876 , GRCh37.p13 chr5: 36,115,149-36,119,978 LMBRD2
    nsv6760525copy number variation1nstd229human GRCh38 chr5: 36,111,570-36,111,658 , GRCh37.p13 chr5: 36,111,672-36,111,760 LMBRD2
    nsv6758314copy number variation1nstd229human GRCh38 chr5: 36,093,901-36,098,400 , GRCh37.p13 chr5: 36,094,003-36,098,502 LMBRD2
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630342copy number variation1nstd224human GRCh37 chr5: 35,694,454-36,110,716 , GRCh38.p12 chr5: 35,694,352-36,110,614 IL7R, SPEF2, 6 more genes
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6561524inversion1nstd223human GRCh38 chr5: 36,131,650-36,132,749 , GRCh37.p13 chr5: 36,131,752-36,132,851 LMBRD2
    nsv6561386inversion1nstd223human GRCh38 chr5: 36,131,666-36,132,880 , GRCh37.p13 chr5: 36,131,768-36,132,982 LMBRD2
    nsv6556341inversion1nstd223human GRCh38 chr5: 36,116,716-36,117,501 , GRCh37.p13 chr5: 36,116,818-36,117,603 LMBRD2
    nsv6382616copy number variation1nstd223human GRCh38 chr5: 36,082,212-36,099,363 , GRCh37.p13 chr5: 36,082,314-36,099,465 LMBRD2
    nsv6381874copy number variation1nstd223human GRCh38 chr5: 36,096,730-36,097,112 , GRCh37.p13 chr5: 36,096,832-36,097,214 LMBRD2
    nsv6380948copy number variation1nstd223human GRCh38 chr5: 36,122,634-36,123,347 , GRCh37.p13 chr5: 36,122,736-36,123,449 LMBRD2
    nsv6380939copy number variation1nstd223human GRCh38 chr5: 36,108,432-36,109,078 , GRCh37.p13 chr5: 36,108,534-36,109,180 LMBRD2
    nsv6377980copy number variation1nstd223human GRCh38 chr5: 36,123,201-36,124,300 , GRCh37.p13 chr5: 36,123,303-36,124,402 LMBRD2
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
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