ntpcr[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
nsv3904470	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 233,020,567-233,225,848 , GRCh38 chr1: 232,884,821-233,090,102 , NCBI36 chr1: 231,087,190-231,292,471	NTPCR, LOC105373201, 3 more genes
nsv6637070	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 233,120,053-233,572,283 , GRCh38.p12 chr1: 232,984,307-233,436,537	NTPCR, MAP3K21, 2 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, LOC105373207, 113 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, 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	NTPCR, LOC105373046, 740 more genes

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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 53

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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