prrg1[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4451713	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 37,281,628-37,377,297 , GRCh38.p12 chrX: 37,422,375-37,518,044	PRRG1, FTH1P27, 2 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	PRRG1, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	PRRG1, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	PRRG1, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	PRRG1, H2AB2, 2152 more genes
nsv3898149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792	PRRG1, OR3B1P, 2154 more genes
nsv3877395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174	PRRG1, ARMCX2, 2154 more genes
nsv3884935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127	PRRG1, NDUFB11, 2154 more genes
nsv3903061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832	PRRG1, SLC38A5, 2152 more genes
nsv3885865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920	PRRG1, MIR1277, 2152 more genes
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	PRRG1, LOC105373176, 2151 more genes
nsv3907545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293	PRRG1, TMEM30BP1, 2151 more genes
nsv3884029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101	PRRG1, SSX4B, 2150 more genes
nsv3898185	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431	PRRG1, ANKRD11P2, 2151 more genes
nsv3891981	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,701-155,978,689 , NCBI36 chrX: 701-154,861,548 , GRCh37 chrX: 60,701-155,208,354	PRRG1, PAICSP7, 2149 more genes
nsv3892026	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 40,904-155,998,166 , GRCh37 chrX: 90,904-155,227,831 , NCBI36 chrX: 30,904-154,881,025	PRRG1, MIR934, 2151 more genes
nsv3903163	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-155,233,731 , GRCh38 chrX: 251,879-156,004,066 , NCBI36 chrX: 108,546-154,886,925	PRRG1, RPL36A, 2151 more genes
nsv3887722	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chrX: 168,546-155,233,731 , GRCh38.p12 chrX: 251,879-156,004,066	PRRG1, CT45A3, 2151 more genes
nsv3901047	copy number variation	3	nstd102	human	Pathogenic, conflicting data from submitters	GRCh38 chrX: 251,880-156,004,066 , GRCh37 chrX: 168,547-155,233,731 , NCBI36 chrX: 108,547-154,886,925	PRRG1, GPR119, 2151 more genes
nsv3890023	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 70,140-154,929,279 , NCBI36 chrX: 10,140-154,582,473 , GRCh38 chrX: 20,140-155,699,618	PRRG1, MIRLET7F2, 2145 more genes

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

Send to:

Search results

Items: 1 to 20 of 152

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 152

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Search details

Recent activity