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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963330copy number variation1nstd209human GRCh38 chr22: 41,565,237-41,566,091 , GRCh37.p13 chr22: 41,961,241-41,962,095 CSDC2
    nsv5948410copy number variation1nstd209human GRCh38 chr22: 41,558,209-41,559,393 , GRCh37.p13 chr22: 41,954,213-41,955,397 LOC105373044, CSDC2
    nsv5549198copy number variation1nstd206human GRCh38 chr22: 41,574,318-41,606,433 , GRCh37.p13 chr22: 41,970,322-42,002,437 CSDC2, DESI1, 1 more genes
    nsv5539302copy number variation1nstd206human GRCh38 chr22: 41,566,586-41,566,882 , GRCh37.p13 chr22: 41,962,590-41,962,886 CSDC2
    nsv5534748copy number variation1nstd206human GRCh38 chr22: 41,566,048-41,566,683 , GRCh37.p13 chr22: 41,962,052-41,962,687 CSDC2
    nsv5328065copy number variation1nstd204human GRCh38.p13 chr22: 41,566,052-41,571,152 , GRCh37.p13 chr22: 41,962,056-41,967,156 CSDC2
    nsv5299062copy number variation1nstd204human GRCh38.p13 chr22: 41,442,501-41,665,900 , GRCh37.p13 chr22: 41,838,505-42,061,904 CSDC2, LOC105373043, 8 more genes
    nsv5297593copy number variation1nstd204human GRCh38.p13 chr22: 41,566,678-41,567,785 , GRCh37.p13 chr22: 41,962,682-41,963,789 CSDC2
    nsv5283344copy number variation1nstd204human GRCh38.p13 chr22: 41,566,811-41,570,623 , GRCh37.p13 chr22: 41,962,815-41,966,627 CSDC2
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 more genes
    nsv5038827copy number variation1nstd200human GRCh38 chr22: 41,566,331-41,606,492 , GRCh37.p13 chr22: 41,962,335-42,002,496 DESI1, CSDC2, 1 more genes
    nsv5038568copy number variation1nstd200human GRCh38 chr22: 41,558,247-41,559,388 , GRCh37.p13 chr22: 41,954,251-41,955,392 CSDC2, LOC105373044
    nsv5034603copy number variation1nstd200human GRCh38 chr22: 41,563,869-41,566,668 , GRCh37.p13 chr22: 41,959,873-41,962,672 CSDC2
    nsv5034188copy number variation1nstd200human GRCh38 chr22: 41,566,492-41,570,810 , GRCh37.p13 chr22: 41,962,496-41,966,814 CSDC2
    nsv5032425inversion1nstd200human GRCh38 chr22: 41,452,969-44,153,937 , GRCh37.p13 chr22: 41,848,973-44,549,817 , LOC101927393, 95 more genes
    nsv4888026copy number variation1nstd200human GRCh37 chr22: 41,970,322-42,002,437 , GRCh38.p12 chr22: 41,574,318-41,606,433 DESI1, CSDC2, 1 more genes
    nsv4887382copy number variation1nstd200human GRCh37 chr22: 41,962,378-41,966,857 , GRCh38.p12 chr22: 41,566,374-41,570,853 CSDC2
    nsv4885769copy number variation1nstd200human GRCh37 chr22: 41,954,660-41,955,079 , GRCh38.p12 chr22: 41,558,656-41,559,075 LOC105373044, CSDC2
    nsv4882439copy number variation1nstd200human GRCh37 chr22: 41,961,582-41,961,834 , GRCh38.p12 chr22: 41,565,578-41,565,830 CSDC2
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
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