prrc1[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
nsv3885433	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 126,644,680-126,938,115 , GRCh38.p12 chr5: 127,308,988-127,602,423	PRRC1, HNRNPKP1, 1 more genes
nsv6636761	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 126,644,681-126,938,115 , GRCh38.p12 chr5: 127,308,989-127,602,423	PRRC1, HNRNPKP1, 1 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	PRRC1, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	PRRC1, TXNDC15, 962 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	PRRC1, LINC01023, 783 more genes
nsv3915450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563	PRRC1, MCTP1, 422 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	PRRC1, LOC105379149, 406 more genes
nsv3924205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 110,023,143-129,439,531 , GRCh38 chr5: 110,687,442-130,103,838 , NCBI36 chr5: 110,051,042-129,467,430	PRRC1, CSNK1G3, 231 more genes
nsv3912712	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 116,677,122-132,686,163 , NCBI36 chr5: 116,040,717-132,049,754 , GRCh37 chr5: 116,012,818-132,021,855	PRRC1, LOC105379149, 185 more genes
nsv6637111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,557,391-128,106,299 , GRCh38.p12 chr5: 113,221,694-128,770,606	PRRC1, SLC12A2, 180 more genes
nsv3920627	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 126,864,591-135,314,282 , GRCh37.p13 chr5: 126,836,692-135,286,383 , GRCh38.p12 chr5: 127,501,000-135,950,694	PRRC1, MIR1289-2, 138 more genes
nsv3910369	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 122,436,202-130,034,178 , GRCh37.p13 chr5: 122,408,303-130,006,279 , GRCh38.p12 chr5: 123,072,608-130,670,586	PRRC1, CSNK1G3, 77 more genes
nsv3911932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 125,774,098-132,209,659 , NCBI36 chr5: 125,801,997-132,237,558 , GRCh38 chr5: 126,438,406-132,873,967	PRRC1, LOC105379176, 93 more genes
nsv6315411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 124,997,035-128,900,524 , GRCh38.p12 chr5: 125,661,342-129,564,831	PRRC1, LOC105379163, 44 more genes
nsv3913517	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 126,458,947-128,537,986 , GRCh37 chr5: 125,794,639-127,873,679 , NCBI36 chr5: 125,822,538-127,901,578	PRRC1, SPMIP10, 28 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	PRRC1, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	PRRC1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	PRRC1, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	PRRC1, PJA2, 1228 more genes
nsv4455983	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762	PRRC1, LOC345576, 419 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 25

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Number of Variants: 20

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