ero1a[All Fields] AND 1[has_clinical] - 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
nsv3916278	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390	ERO1A, LOC105370507, 98 more genes
nsv3913833	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 51,081,314-54,857,069 , GRCh38 chr14: 51,544,846-55,320,598 , GRCh37 chr14: 52,011,564-55,787,316	ERO1A, SOCS4, 65 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, 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	ERO1A, ARF6, 219 more genes
nsv3896365	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 52,890,163-53,288,450 , GRCh38.p12 chr14: 52,423,445-52,821,732	ERO1A, PSMC6, 6 more genes
nsv3895079	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 53,077,252-53,557,861 , GRCh38.p12 chr14: 52,610,534-53,091,143	ERO1A, GNPNAT1, 8 more genes

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