creg1[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
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	CREG1, CRB1, 1608 more genes
nsv3873192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589	CREG1, COLGALT2, 402 more genes
nsv3889882	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847	CREG1, FMO4, 403 more genes
nsv4346684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189	CREG1, LINC00626, 359 more genes
nsv3901593	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022	CREG1, NME7, 233 more genes
nsv3894431	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154	CREG1, RPL21P27, 238 more genes
nsv6313719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192	CREG1, LOC100420658, 167 more genes
nsv3904950	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 166,762,832-175,327,423 , NCBI36 chr1: 164,998,693-173,563,182 , GRCh37 chr1: 166,732,069-175,296,559	CREG1, LINC01681, 186 more genes
nsv4674768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480	CREG1, ATP1B1, 156 more genes
nsv4453493	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 163,093,021-168,991,239 , GRCh38.p12 chr1: 163,123,231-169,022,001	CREG1, RNU6-755P, 101 more genes
nsv6313602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473	CREG1, DCAF6, 101 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	CREG1, 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	CREG1, 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	CREG1, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	CREG1, LOC101060227, 1608 more genes
nsv3900459	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332	CREG1, HORMAD1, 923 more genes
nsv3890224	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 157,747,246-176,021,247 , GRCh37 chr1: 157,717,036-175,990,383 , NCBI36 chr1: 155,983,660-174,257,006	CREG1, LOC101928596, 475 more genes
nsv3896331	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 164,922,655-180,061,589 , NCBI36 chr1: 163,158,516-178,297,347 , GRCh37 chr1: 164,891,892-180,030,724	CREG1, GAS5-AS1, 290 more genes
nsv4728711	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 164,608,682-169,216,098 , GRCh38.p12 chr1: 164,639,445-169,246,860	CREG1, ALDH9A1, 95 more genes
nsv4674180	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 166,284,108-167,681,975 , GRCh38.p12 chr1: 166,314,871-167,712,738	CREG1, CNN2P10, 28 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 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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