prrx1[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
nsv3898794	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 168,525,390-168,991,920 , GRCh38 chr1: 170,289,625-170,756,155 , GRCh37 chr1: 170,258,766-170,725,296	PRRX1, GORAB-AS1, 3 more genes
nsv4728742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 170,503,528-170,666,132 , GRCh38.p12 chr1: 170,534,387-170,696,991	PRRX1, LOC105371610, 1 more genes
nsv4454258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 170,519,336-170,666,165 , GRCh38.p12 chr1: 170,550,195-170,697,024	PRRX1, LOC105371610, 1 more genes
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	PRRX1, CRB1, 1608 more genes
nsv3873192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589	PRRX1, COLGALT2, 402 more genes
nsv3901149	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 168,271,833-185,790,903 , GRCh37 chr1: 170,005,209-187,524,280 , GRCh38 chr1: 170,036,068-187,555,148	PRRX1, RGSL1, 296 more genes
nsv3889882	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847	PRRX1, FMO4, 403 more genes
nsv4346684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189	PRRX1, LINC00626, 359 more genes
nsv3901593	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022	PRRX1, NME7, 233 more genes
nsv3894431	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154	PRRX1, RPL21P27, 238 more genes
nsv3885424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,873,155-181,823,980 , GRCh38.p12 chr1: 169,904,014-181,854,845	PRRX1, TRUND-NNN7-1, 210 more genes
nsv6313719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192	PRRX1, LOC100420658, 167 more genes
nsv3896314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,187,474-178,044,969 , NCBI36 chr1: 167,454,098-176,311,592 , GRCh38 chr1: 169,218,236-178,075,834	PRRX1, RPS26P12, 150 more genes
nsv3904950	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 166,762,832-175,327,423 , NCBI36 chr1: 164,998,693-173,563,182 , GRCh37 chr1: 166,732,069-175,296,559	PRRX1, LINC01681, 186 more genes
nsv4674768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480	PRRX1, ATP1B1, 156 more genes
nsv3893479	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 166,550,684-173,535,058 , GRCh38 chr1: 168,314,822-175,299,299 , GRCh37 chr1: 168,284,060-175,268,435	PRRX1, GORAB-AS1, 147 more genes
nsv3885421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,095,250-175,778,910 , GRCh38.p12 chr1: 169,126,012-175,809,774	PRRX1, ZBTB37, 130 more genes
nsv6313602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473	PRRX1, DCAF6, 101 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	PRRX1, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	PRRX1, SNAP47, 4927 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 27

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Number of Variants: 20

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