arg2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	ARG2, 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	ARG2, 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	ARG2, 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	ARG2, 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	ARG2, 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	ARG2, 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	ARG2, 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	ARG2, PAPOLA-DT, 1338 more genes
nsv3903706	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 68,035,240-73,568,130 , GRCh38.p12 chr14: 67,568,523-73,101,422	ARG2, ACTN1, 108 more genes
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	ARG2, ACTN1, 400 more genes
nsv5380972	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr14: 65,937,790-68,354,021 , GRCh38.p12 chr14: 65,471,072-67,887,304	ARG2, RPL21P9, 35 more genes
nsv4675709	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 67,331,167-68,451,970 , GRCh38.p12 chr14: 66,864,449-67,985,253	ARG2, RDH11, 25 more genes
nsv6314209	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 67,443,801-68,153,682 , GRCh38.p12 chr14: 66,977,084-67,686,965	ARG2, PLEK2, 18 more genes
nsv4675260	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 68,037,409-68,278,365 , GRCh38.p12 chr14: 67,570,692-67,811,648	ARG2, PLEKHH1, 13 more genes
nsv4436741	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 68,110,557-68,283,783 , GRCh38.p12 chr14: 67,643,840-67,817,066	ARG2, RN7SL213P, 9 more genes

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