pole2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6309756	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 50,131,805-50,133,151 , GRCh38.p12 chr14: 49,665,087-49,666,433	POLE2
nsv6309351	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 50,154,834-50,154,921 , GRCh38.p12 chr14: 49,688,116-49,688,203	POLE2
nsv3909218	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 50,073,908-50,127,672 , GRCh38.p12 chr14: 49,607,190-49,660,954	POLE2, MGAT2, 3 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	POLE2, HNRNPC, 616 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	POLE2, LOC440181, 1998 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	POLE2, BANF1P1, 1996 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	POLE2, LOC100289511, 1996 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	POLE2, DHRS7, 1946 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	POLE2, SRMP2, 1929 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	POLE2, CRIP1, 1929 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	POLE2, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	POLE2, PAPOLA-DT, 1338 more genes
nsv3911849	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461	POLE2, ARF6, 219 more genes
nsv3902764	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 50,069,088-50,199,169 , GRCh38.p12 chr14: 49,602,370-49,732,451	POLE2, RPL36AL, 6 more genes
nsv6309547	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 50,050,385-50,118,115 , GRCh38.p12 chr14: 49,583,667-49,651,397	POLE2, RHOQP1, 6 more genes
nsv6314025	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 45,827,312-50,529,931 , GRCh38.p12 chr14: 45,358,109-50,063,213	POLE2, RPL18P1, 52 more genes

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pole2[All Fields] AND 1[has_clinical] (17)
dbVar
Absent radius
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