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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5643272insertion1nstd207human GRCh38 chr9: 130,901,254-130,901,254 , GRCh37.p13 chr9: 133,776,641-133,776,641 FIBCD1
    nsv5491556copy number variation1nstd206human GRCh38 chr9: 130,909,746-130,917,372 , GRCh37.p13 chr9: 133,785,133-133,792,759 FIBCD1
    nsv5486741copy number variation1nstd206human GRCh38 chr9: 130,876,725-130,992,635 , GRCh37.p13 chr9: 133,752,112-133,868,022 FIBCD1-AS1, QRFP, 2 more genes
    nsv5330158translocation1nstd200human GRCh37 chr9: 133,788,730-133,788,730 , GRCh37 chr9: 133,788,435-133,788,435 , GRCh38.p12 chr9: 130,913,048-130,913,048 , GRCh38.p12 chr9: 130,913,343-130,913,343 FIBCD1
    nsv4988543copy number variation1nstd200human GRCh38 chr9: 130,932,435-130,938,507 , GRCh37.p13 chr9: 133,807,822-133,813,894 FIBCD1, FIBCD1-AS1
    nsv4988542copy number variation1nstd200human GRCh38 chr9: 130,928,009-130,946,037 , GRCh37.p13 chr9: 133,803,396-133,821,424 FIBCD1, FIBCD1-AS1
    nsv4988541copy number variation1nstd200human GRCh38 chr9: 130,918,643-130,920,560 , GRCh37.p13 chr9: 133,794,030-133,795,947 FIBCD1
    nsv4985779copy number variation1nstd200human GRCh38 chr9: 130,904,662-130,911,859 , GRCh37.p13 chr9: 133,780,049-133,787,246 FIBCD1
    nsv4681157copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,540,031-134,398,503 , GRCh38.p12 chr9: 130,664,644-131,523,116 LOC105376299, FIBCD1-AS1, 19 more genes
    nsv4666387copy number variation1nstd186human GRCh37 chr9: 133,785,166-133,792,756 , GRCh38.p12 chr9: 130,909,779-130,917,369 FIBCD1
    nsv4616987copy number variation1nstd183human GRCh37 chr9: 133,785,166-133,792,756 , GRCh38.p12 chr9: 130,909,779-130,917,369 FIBCD1
    nsv4551429insertion1nstd166human GRCh37.p13 chr9: 133,805,811-133,805,811 , GRCh38.p12 chr9: 130,930,424-130,930,424 FIBCD1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456810copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,276,056-133,851,405 , GRCh38.p12 chr9: 130,400,669-130,976,018 ABL1, PRDM12, 13 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4428571copy number variation1nstd174human GRCh37 chr9: 133,752,128-133,868,045 , GRCh38.p12 chr9: 130,876,741-130,992,658 ABL1, FIBCD1, 2 more genes
    nsv4413973copy number variation1nstd174human GRCh37 chr9: 133,785,055-133,792,895 , GRCh38.p12 chr9: 130,909,668-130,917,508 FIBCD1
    nsv4349353copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684 ABL1, ASS1, 69 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4188959copy number variation1nstd166human GRCh37.p13 chr9: 133,805,749-133,805,814 , GRCh38.p12 chr9: 130,930,362-130,930,427 FIBCD1
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