hspd1[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
nsv3915836	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 19,161,100-19,400,011 , GRCh38 chr5: 19,125,234-19,364,145 , GRCh37 chr5: 19,125,343-19,364,254	HSPD1P15
nsv3886866	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 19,085,981-19,322,752 , GRCh38.p12 chr5: 19,085,872-19,322,643	HSPD1P15
nsv3910103	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 19,032,921-19,344,577 , GRCh37.p13 chr5: 18,997,164-19,308,820 , GRCh38.p12 chr5: 18,997,055-19,308,711	HSPD1P15, RPL32P14
nsv3911217	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 19,032,921-19,325,652 , GRCh37.p13 chr5: 18,997,164-19,289,895 , GRCh38.p12 chr5: 18,997,055-19,289,786	HSPD1P15, RPL32P14
nsv3921655	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 145,893,771-146,112,549 , GRCh37.p13 chr4: 145,674,321-145,893,099 , GRCh38.p12 chr4: 144,753,169-144,971,947	ANAPC10, HSPD1P5
nsv7096596	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 198,351,770-198,351,942 , GRCh38.p12 chr2: 197,487,046-197,487,218	HSPD1, SNORA105B
nsv3915624	copy number variation	1	nstd102	human	Benign	NCBI36 chr5: 21,907,898-22,192,403 , GRCh37 chr5: 21,872,141-22,156,646 , GRCh38 chr5: 21,872,032-22,156,537	CDH12, PMCHL1, 3 more genes
nsv3888330	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 18,997,080-20,081,779 , GRCh38.p12 chr5: 18,996,971-20,081,670	LOC105374672, RPL32P14, 2 more genes
nsv3912606	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr13: 37,976,312-38,558,676 , NCBI36 chr13: 37,448,449-38,030,813 , GRCh37 chr13: 38,550,449-39,132,813	HSPD1P9, UFM1, 3 more genes
nsv3917736	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr4: 144,701,081-145,042,652 , NCBI36 chr4: 145,841,683-146,183,254 , GRCh37 chr4: 145,622,233-145,963,804	HSPD1P5, HHIP, 2 more genes
nsv3888889	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 19,054,487-19,790,210 , GRCh38.p12 chr5: 19,054,378-19,790,101	HSPD1P15, CDH18, 1 more genes
nsv4457117	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 105,126,026-105,861,393 , GRCh38.p12 chr11: 105,255,299-105,990,666	RNU6-277P, RNU4-55P, 3 more genes
nsv4729717	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 145,739,988-145,986,668 , GRCh38.p12 chr4: 144,818,836-145,065,516	RN7SKP235, ANAPC10, 1 more genes
nsv3921111	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 21,852,834-21,964,183 , NCBI36 chr5: 21,888,591-21,999,940 , GRCh38 chr5: 21,852,725-21,964,074	CDH12, SNORA105A, 2 more genes
nsv4456943	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 19,071,213-20,241,053 , GRCh38.p12 chr5: 19,071,104-20,240,944	CDH18, HSPD1P15, 1 more genes
nsv4729669	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 19,101,001-20,164,000 , GRCh38.p12 chr5: 19,100,892-20,163,891	HSPD1P15, CDH18, 1 more genes
nsv3877376	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 135,699,216-136,201,487 , GRCh38.p12 chr5: 136,363,528-136,865,798	ANKRD49P3, HNRNPA1P13, 3 more genes
nsv6290880	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 135,699,216-136,197,957 , GRCh38.p12 chr5: 136,363,528-136,862,268	HNRNPA1P13, ANKRD49P3, 3 more genes
nsv4674251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 145,601,590-146,031,966 , GRCh38.p12 chr4: 144,680,438-145,110,814	HSPD1P5, ABCE1, 3 more genes
nsv3884752	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr2: 197,487,026-197,498,868 , GRCh37.p13 chr2: 198,351,750-198,363,592	HSPD1, HSPE1-MOB4, 2 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 825

Page of 42

Number of Variants: 20

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Supplemental Content

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