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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6777951copy number variation1nstd229human GRCh38 chr5: 59,470,501-59,737,500 , GRCh37.p13 chr5: 58,766,327-59,033,326 LOC107986347, NDUFB4P2, 2 more genes
    nsv6773854copy number variation1nstd229human GRCh38 chr5: 59,328,293-59,704,080 , GRCh37.p13 chr5: 58,624,119-58,999,906 PDE4D, NDUFB4P2, 2 more genes
    nsv6758499copy number variation1nstd229human GRCh38 chr5: 59,360,907-59,715,093 , GRCh37.p13 chr5: 58,656,733-59,010,919 LOC107986347, NDUFB4P2, 2 more genes
    nsv6567227inversion1nstd223human GRCh38 chr5: 59,702,152-59,702,658 , GRCh37.p13 chr5: 58,997,978-58,998,484 MIR582, PDE4D
    nsv6406645copy number variation1nstd223human GRCh38 chr5: 59,703,301-59,705,800 , GRCh37.p13 chr5: 58,999,127-59,001,626 PDE4D, MIR582
    nsv6135422copy number variation1nstd213human GRCh37 chr5: 58,800,000-59,200,001 , GRCh38.p12 chr5: 59,504,174-59,904,174 PDE4D, MIR582, 4 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135187copy number variation1nstd213human GRCh37 chr5: 58,690,000-59,250,001 , GRCh38.p12 chr5: 59,394,174-59,954,174 PDE4D, MIR582, 4 more genes
    nsv4803138copy number variation1nstd200human GRCh37 chr5: 58,963,882-59,019,527 , GRCh38.p12 chr5: 59,668,056-59,723,701 PDE4D, MIR582
    nsv4729528copy number variation1nstd102humanUncertain significance GRCh37 chr5: 58,932,935-59,044,761 , GRCh38.p12 chr5: 59,637,109-59,748,935 PDE4D, MIR582
    nsv4679866copy number variation1nstd189human GRCh37.p13 chr5: 58,964,395-59,910,320 , GRCh38.p12 chr5: 59,668,569-60,614,493 PDE4D, PART1, 7 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4128054copy number variation1nstd166human GRCh37.p13 chr5: 58,963,882-59,019,527 , GRCh38.p12 chr5: 59,668,056-59,723,701 MIR582, PDE4D
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv4115627copy number variation1nstd166human GRCh37.p13 chr5: 58,993,600-59,008,168 , GRCh38.p12 chr5: 59,697,774-59,712,342 MIR582, PDE4D
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3919888copy number variation1nstd102humanUncertain significance NCBI36 chr5: 58,998,125-59,122,299 , GRCh37.p13 chr5: 58,962,368-59,086,542 , GRCh38.p12 chr5: 59,666,542-59,790,716 MIR582, PDE4D, 1 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
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