dbVar for OMIM (Select 607210) - dbVar - NCBI

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Items: 5

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Number of Variants: 5

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4683171	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,946,252-2,957,039 , GRCh38.p12 chr7: 2,906,618-2,917,405	CARD11
nsv4682835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 2,983,826-2,987,441 , GRCh38.p12 chr7: 2,944,192-2,947,807	CARD11, CARD11-AS1
nsv4681148	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 2,962,248-2,998,160 , GRCh38.p12 chr7: 2,922,614-2,958,526	CARD11-AS1, CARD11
nsv4450888	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 2,906,618-2,958,526 , GRCh37 chr7: 2,946,252-2,998,160	CARD11-AS1, CARD11
nsv3871344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 2,914,850-2,916,262 , GRCh37.p13 chr7: 2,954,484-2,955,896	CARD11

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