psma1[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
nsv3903491	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 14,657,389-14,918,308 , GRCh38.p12 chr11: 14,635,843-14,896,762	PSMA1, PDE3B, 3 more genes
nsv3901984	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 14,508,698-14,865,666 , GRCh38.p12 chr11: 14,487,152-14,844,120	PSMA1, LOC107984315, 3 more genes
nsv3924101	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 14,616,544-14,828,528 , NCBI36 chr11: 14,573,120-14,785,104 , GRCh38 chr11: 14,594,998-14,806,982	PSMA1, LOC107984315, 2 more genes
nsv4457233	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 14,513,629-14,816,556 , GRCh38.p12 chr11: 14,492,083-14,795,010	PSMA1, MORF4L1P3, 3 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	PSMA1, FAUP4, 2031 more genes
nsv3915585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806	PSMA1, BTBD10, 86 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	PSMA1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	PSMA1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	PSMA1, IGHMBP2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	PSMA1, OR51L1, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	PSMA1, BGLT3, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	PSMA1, PCNAP4, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	PSMA1, OR52Q1P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	PSMA1, SDHCP4, 620 more genes
nsv4674824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344	PSMA1, SNORA88, 305 more genes
nsv3912558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865	PSMA1, TRIM22, 546 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	PSMA1, MTND5P21, 506 more genes
nsv4675502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341	PSMA1, MRGPRX5P, 171 more genes
nsv3894954	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 14,504,463-14,909,461 , GRCh38.p12 chr11: 14,482,917-14,887,915	PSMA1, COPB1, 4 more genes
nsv3891007	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 14,498,547-14,855,923 , GRCh38.p12 chr11: 14,477,001-14,834,377	PSMA1, PDE3B, 4 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 24

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Number of Variants: 20

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Search details

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