dbVar for Gene (Select 5693) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4729365	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 23,457,638-23,698,285 , GRCh38.p12 chr14: 22,988,429-23,229,076	RNF212B, CDH24, 13 more genes
nsv4685750	copy number variation	1	nstd102	human	not provided	GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685	IGBP1P1, RAB2B, 579 more genes
nsv4675943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827	TRAJ36, SEC23A-AS1, 590 more genes
nsv4578270	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011	BCL2L2, CEBPE, 215 more genes
nsv4349901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881	TRAV4, UNGP2, 458 more genes
nsv3922265	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120	ANG, APEX1, 346 more genes
nsv3920885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,619,308-23,911,404 , NCBI36 chr14: 19,689,148-22,981,244 , GRCh38 chr14: 20,151,149-23,442,195	SLC39A2, APEX1, 294 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	SRMP2, IGHV3-71, 1929 more genes
nsv3918965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625	TRAJ13, LRP10, 589 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	MIR656, TRAJ59, 1918 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	MIR208B, MRPL52, 600 more genes
nsv3913204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995	SMARCE1P3, LOC100421646, 635 more genes
nsv3912710	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,000,611-38,984,415 , NCBI36 chr14: 19,538,610-38,523,370 , GRCh37 chr14: 20,468,770-39,453,619	UBE2NP1, MIR4307HG, 553 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	BANF1P1, IGHV1-68, 1996 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	CRIP1, GPATCH2L, 1929 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	DHRS7, MIR548Y, 1946 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	LOC440181, HEATR5A-DT, 1998 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	LOC100289511, RNU6-552P, 1996 more genes
nsv3898685	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-34,049,214 , GRCh38.p12 chr14: 19,652,445-33,580,008	LOC105370419, SNORD126, 480 more genes
nsv3898291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-27,768,254 , GRCh38.p12 chr14: 19,652,445-27,299,048	HOMEZ, RNU6-1138P, 411 more genes

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Number of Variants: 20

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