coa6[All Fields] AND 1[has_clinical] - 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
nsv4453777	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 234,479,682-234,518,218 , GRCh38.p12 chr1: 234,343,936-234,382,472	COA6, RPS15P2, 1 more genes
nsv4453443	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 234,491,689-234,518,218 , GRCh38.p12 chr1: 234,355,943-234,382,472	COA6, RPS15P2, 1 more genes
nsv6634337	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719	COA6, OR2M4, 316 more genes
nsv3904200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 230,106,271-243,677,283 , NCBI36 chr1: 228,308,641-241,907,208 , GRCh37 chr1: 230,242,018-243,840,585	COA6, MIR3123, 221 more genes
nsv7148175	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437	COA6, AGT, 221 more genes
nsv4674115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061	COA6, LOC105373163, 258 more genes
nsv6636217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914	COA6, LINC01347, 169 more genes
nsv3912845	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 230,713,047-240,722,962 , GRCh37.p13 chr1: 232,646,424-242,656,339 , GRCh38.p12 chr1: 232,510,678-242,493,037	COA6, RNU4-77P, 158 more genes
nsv3881799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 232,226,609-241,010,904 , GRCh38.p12 chr1: 232,090,863-240,847,604	COA6, MIPEPP2, 137 more genes
nsv6112661	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559	COA6, LOC105373207, 113 more genes
nsv4674008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 233,843,930-237,971,511 , GRCh38.p12 chr1: 233,708,184-237,808,211	COA6, LGALS8-AS1, 75 more genes
nsv7137173	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319	COA6, ARID4B, 58 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	COA6, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	COA6, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	COA6, RNU1-153P, 4887 more genes
nsv4450583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041	COA6, RGS18, 1186 more genes
nsv3881012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 195,483,439-249,213,000 , GRCh38.p12 chr1: 195,514,309-248,918,801	COA6, LOC105372928, 1062 more genes
nsv6634372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485	COA6, LOC105373279, 1036 more genes
nsv4674140	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793	COA6, RNA5S8, 893 more genes
nsv3897747	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 207,346,642-248,930,485 , GRCh37 chr1: 207,519,987-249,224,684 , NCBI36 chr1: 205,586,610-247,191,307	COA6, RPS18P3, 793 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 55

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Number of Variants: 20

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Supplemental Content

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Search details

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