pacrg[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
nsv3898789	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,239,119-163,307,736 , GRCh38.p12 chr6: 162,818,087-162,886,704	PACRG
nsv3895312	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,447,714-163,496,289 , GRCh38.p12 chr6: 163,026,682-163,075,257	PACRG, PACRG-AS2
nsv3896345	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,144,683-163,176,151 , GRCh38.p12 chr6: 162,723,651-162,755,119	PACRG, PRKN
nsv3908891	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,171,970-163,259,260 , GRCh38.p12 chr6: 162,750,938-162,838,228	PACRG, TRE-TTC15-1
nsv3906024	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,103,748-163,151,824 , GRCh38.p12 chr6: 162,682,716-162,730,792	PACRG, PRKN
nsv3902568	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 163,710,391-163,747,722 , GRCh38.p12 chr6: 163,289,359-163,326,690	PACRG, PACRG-AS1
nsv3924794	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 163,161,575-163,350,535 , GRCh37.p13 chr6: 163,241,585-163,430,545 , GRCh38.p12 chr6: 162,820,553-163,009,513	PACRG, RPL34P15
nsv3922683	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 162,970,390-163,126,258 , GRCh37.p13 chr6: 163,050,400-163,206,268 , GRCh38.p12 chr6: 162,629,368-162,785,236	PACRG, PRKN
nsv6312471	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,683,537-163,148,700 , GRCh38.p12 chr6: 162,262,505-162,727,668	PACRG, PRKN, 2 more genes
nsv3876327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 162,262,766-162,727,661 , GRCh37.p13 chr6: 162,683,798-163,148,693	PACRG, PRKN, 2 more genes
nsv5674232	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr6: 162,683,772-163,146,228 , GRCh38.p12 chr6: 162,262,740-162,725,196	PACRG, PRKN, 2 more genes
nsv6315287	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,683,798-163,148,693 , GRCh38.p12 chr6: 162,262,766-162,727,661	PACRG, PRKN, 2 more genes
nsv3880107	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr6: 162,609,404-162,813,090 , GRCh37.p13 chr6: 163,030,436-163,234,122	PACRG, PRKN, 1 more genes
nsv6314330	complex chromosomal rearrangement	7	nstd102	human	Likely pathogenic	GRCh37 chr2: 153,546,999-153,546,999 , GRCh37 chr2: 153,547,028-153,547,028 , GRCh37 chr5: 124,175,407-124,175,407 , GRCh37 chr5: 124,176,058-124,176,058 , GRCh37 chr5: 125,626,214-125,626,214 , GRCh37 chr5: 125,626,285-125,626,285 , GRCh37 chr6: 128,463,242-128,463,242 , GRCh37 chr6: 128,463,306-128,463,306 , GRCh37 chr6: 128,511,150-128,511,150 , GRCh37 chr6: 128,511,189-128,511,189 , GRCh37 chr6: 163,472,151-163,472,151 , GRCh37 chr6: 163,472,169-163,472,169 , GRCh37 chr7: 127,652,521-127,652,521 , GRCh37 chr7: 127,652,531-127,652,531 , GRCh38.p12 chr2: 152,690,485-152,690,485 , GRCh38.p12 chr2: 152,690,514-152,690,514 , GRCh38.p12 chr5: 124,839,714-124,839,714 , GRCh38.p12 chr5: 124,840,365-124,840,365 , GRCh38.p12 chr5: 126,290,522-126,290,522 , GRCh38.p12 chr5: 126,290,593-126,290,593 , GRCh38.p12 chr6: 128,142,097-128,142,097 , GRCh38.p12 chr6: 128,142,161-128,142,161 , GRCh38.p12 chr6: 128,190,005-128,190,005 , GRCh38.p12 chr6: 128,190,044-128,190,044 , GRCh38.p12 chr6: 163,051,119-163,051,119 , GRCh38.p12 chr6: 163,051,137-163,051,137 , GRCh38.p12 chr7: 128,012,468-128,012,468 , GRCh38.p12 chr6\|NT_187556.1: 539,378-539,378 , GRCh38.p12 chr6\|NT_187556.1: 491,431-491,431 , GRCh38.p12 chr7: 128,012,478-128,012,478 , GRCh38.p12 chr6\|NT_187556.1: 491,495-491,495 , GRCh38.p12 chr6\|NT_187556.1: 539,339-539,339	PACRG, PTPRK, 3 more genes
nsv3920046	copy number variation	1	nstd102	human	Benign	NCBI36 chr6: 163,049,454-163,436,441 , GRCh37 chr6: 163,129,464-163,516,451 , GRCh38 chr6: 162,708,432-163,095,419	PACRG, RPL34P15, 3 more genes
nsv3902430	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 163,596,914-163,779,357 , GRCh38.p12 chr6: 163,175,882-163,358,325	PACRG, PACRG-AS3, 3 more genes
nsv4456170	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 162,672,841-163,349,274 , GRCh38.p12 chr6: 162,251,809-162,928,242	PACRG, KRT8P44, 3 more genes
nsv3901309	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 162,754,605-163,163,098 , GRCh38.p12 chr6: 162,333,573-162,742,066	PACRG, PRKN, 2 more genes
nsv3915090	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 163,337,791-163,606,120 , NCBI36 chr6: 163,257,781-163,526,110 , GRCh38 chr6: 162,916,759-163,185,088	PACRG, PACRG-AS2, 2 more genes
nsv3915532	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 162,124,839-162,738,363 , NCBI36 chr6: 162,465,861-163,079,385 , GRCh37 chr6: 162,545,871-163,159,395	PACRG, KRT8P44, 3 more genes

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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 88

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Number of Variants: 20

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