dbVar for OMIM (Select 609524) - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5674026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 128,469,483-128,500,328 , GRCh38.p12 chr7: 128,829,429-128,860,274	FLNC, FLNC-AS1
nsv5673787	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 128,475,370-128,478,867 , GRCh38.p12 chr7: 128,835,316-128,838,813	FLNC
nsv5381397	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,470,672-128,498,597 , GRCh38.p12 chr7: 128,830,618-128,858,543	FLNC-AS1, FLNC
nsv4682955	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,475,370-128,498,587 , GRCh38.p12 chr7: 128,835,316-128,858,533	FLNC-AS1, FLNC
nsv4682891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 128,488,605-128,489,046 , GRCh38.p12 chr7: 128,848,551-128,848,992	FLNC-AS1, FLNC
nsv4681823	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,482,275-128,490,138 , GRCh38.p12 chr7: 128,842,221-128,850,084	FLNC, FLNC-AS1
nsv4681161	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr7: 128,470,682-128,498,587 , GRCh38.p12 chr7: 128,830,628-128,858,533	FLNC, FLNC-AS1
nsv4681077	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,498,380-128,498,587 , GRCh38.p12 chr7: 128,858,326-128,858,533	FLNC-AS1, FLNC
nsv4452758	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,498,052-128,498,587 , GRCh38 chr7: 128,857,998-128,858,533	FLNC-AS1, FLNC
nsv4450159	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 128,492,635-128,498,587 , GRCh38 chr7: 128,852,581-128,858,533	FLNC, FLNC-AS1
nsv3884554	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 128,830,618-128,858,543 , GRCh37 chr7: 128,470,672-128,498,597	FLNC, FLNC-AS1
nsv3881277	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 128,858,008-128,858,217 , GRCh37.p13 chr7: 128,498,062-128,498,271	FLNC, FLNC-AS1
nsv3873633	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 128,857,988-128,858,543 , GRCh37 chr7: 128,498,042-128,498,597	FLNC-AS1, FLNC

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