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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6875009copy number variation1nstd229human GRCh38 chr9: 83,640,429-83,643,237 , GRCh37.p13 chr9: 86,255,344-86,258,152 IDNK
    nsv6872245copy number variation1nstd229human GRCh38 chr9: 83,639,002-83,640,913 , GRCh37.p13 chr9: 86,253,917-86,255,828 IDNK
    nsv6871334copy number variation1nstd229human GRCh38 chr9: 83,625,420-83,628,438 , GRCh37.p13 chr9: 86,240,335-86,243,353 IDNK
    nsv6871233copy number variation1nstd229human GRCh38 chr9: 83,550,494-83,641,177 , GRCh37.p13 chr9: 86,165,409-86,256,092 IDNK, FRMD3, 1 more genes
    nsv6864314copy number variation1nstd229human GRCh38 chr9: 83,641,755-83,646,495 , GRCh37.p13 chr9: 86,256,670-86,261,410 IDNK
    nsv6637221copy number variation1nstd102humanUncertain significance GRCh37 chr9: 86,228,495-86,434,873 , GRCh38.p12 chr9: 83,613,580-83,819,958 IDNK, UBQLN1-AS1, 3 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633934copy number variation1nstd224human GRCh37 chr9: 86,195,933-86,399,815 , GRCh38.p12 chr9: 83,581,018-83,784,900 UBQLN1, GKAP1, 4 more genes
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6454291copy number variation1nstd223human GRCh38 chr9: 83,639,002-83,640,913 , GRCh37.p13 chr9: 86,253,917-86,255,828 IDNK
    nsv6442124copy number variation1nstd223human GRCh38 chr9: 83,641,457-83,643,082 , GRCh37.p13 chr9: 86,256,372-86,257,997 IDNK
    nsv6436228copy number variation1nstd223human GRCh38 chr9: 83,594,348-83,648,913 , GRCh37.p13 chr9: 86,209,263-86,263,828 IDNK, RNU4-15P
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314047copy number variation1nstd102humanUncertain significance GRCh37 chr9: 85,704,023-86,455,979 , GRCh38.p12 chr9: 83,089,108-83,841,064 UBQLN1-AS1, IDNK, 9 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv5490829copy number variation1nstd206human GRCh38 chr9: 83,627,049-83,627,130 , GRCh37.p13 chr9: 86,241,964-86,242,045 IDNK
    nsv5372708translocation1nstd200human GRCh38 chr9: 83,623,117-83,623,117 , GRCh38 chr9: 83,623,177-83,623,177 , GRCh37.p13 chr9: 86,238,092-86,238,092 , GRCh37.p13 chr9: 86,238,032-86,238,032 IDNK
    nsv5132662mobile element insertion1nstd203human GRCh38 chr9: 83,625,981-83,625,992 , GRCh37.p13 chr9: 86,240,896-86,240,907 IDNK
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