capn2[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
nsv3900990	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr1: 223,742,902-223,749,425 , GRCh37 chr1: 223,930,604-223,937,127 , NCBI36 chr1: 221,997,227-222,003,750	CAPN2
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	CAPN2, LOC105373163, 258 more genes
nsv4674157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,641,389-228,137,574 , GRCh38.p12 chr1: 222,468,047-227,949,873	CAPN2, SRP9, 123 more genes
nsv3908695	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 221,587,658-226,810,656 , GRCh38 chr1: 223,347,693-228,556,332 , GRCh37 chr1: 223,521,035-228,744,033	CAPN2, SNAP47, 137 more genes
nsv4674721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 219,734,913-224,104,993 , GRCh38.p12 chr1: 219,561,571-223,917,291	CAPN2, PRELID3BP1, 82 more genes
nsv4728176	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 222,605,125-224,696,628 , GRCh38.p12 chr1: 222,431,783-224,508,926	CAPN2, SEPTIN7P13, 52 more genes
nsv5200338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,552,998-224,761,890 , GRCh38.p12 chr1: 223,379,656-224,574,188	CAPN2, LOC105373025, 32 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	CAPN2, 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	CAPN2, 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	CAPN2, 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	CAPN2, 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	CAPN2, 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	CAPN2, 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	CAPN2, 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	CAPN2, RPS18P3, 793 more genes
nsv3890682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 209,819,552-249,225,312 , NCBI36 chr1: 207,886,175-247,191,935 , GRCh38 chr1: 209,646,207-248,931,113	CAPN2, HLX, 749 more genes
nsv3892818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 209,963,625-248,918,469 , GRCh37 chr1: 210,136,970-249,212,668 , NCBI36 chr1: 208,203,593-247,179,291	CAPN2, LOC105373046, 740 more genes
nsv4684187	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793	CAPN2, HLX-AS1, 740 more genes
nsv3895767	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 187,143,981-224,299,417 , NCBI36 chr1: 185,379,736-222,553,742 , GRCh37 chr1: 187,113,113-224,487,119	CAPN2, LOC107985458, 590 more genes
nsv3892503	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 212,263,778-247,179,291 , GRCh38 chr1: 214,023,812-248,918,469 , GRCh37 chr1: 214,197,155-249,212,668	CAPN2, HMGN2P19, 672 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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