gpr161[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
nsv4454005	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 102,504,143-102,550,116 , GRCh37 chr10: 104,263,900-104,309,873	SUFU
nsv5380786	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,386,922-104,392,580 , GRCh38.p12 chr10: 102,627,165-102,632,823	SUFU
nsv3884253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,353,387-104,357,056 , GRCh38 chr10: 102,593,630-102,597,299	SUFU
nsv5672605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,352,329-104,353,832 , GRCh38.p12 chr10: 102,592,572-102,594,075	SUFU
nsv5672685	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,352,329-104,352,491 , GRCh38.p12 chr10: 102,592,572-102,592,734	SUFU
nsv4452213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,309,717-104,309,873 , GRCh38 chr10: 102,549,960-102,550,116	SUFU
nsv6309054	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 104,352,329-104,377,195 , GRCh38.p12 chr10: 102,592,572-102,617,438	SUFU
nsv7093102	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr10: 104,377,195-104,377,273 , GRCh38 chr10: 102,617,438-102,617,516	SUFU
nsv6308976	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 104,375,015-104,389,912 , GRCh38.p12 chr10: 102,615,258-102,630,155	SUFU
nsv7093856	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 104,262,628-104,309,873 , GRCh38.p12 chr10: 102,502,871-102,550,116	SUFU, ACTR1A
nsv6308897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 104,263,900-104,389,922 , GRCh38.p12 chr10: 102,504,143-102,630,165	RNU6-43P, SUFU, 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	GPR161, 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	GPR161, COLGALT2, 402 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	GPR161, 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	GPR161, 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	GPR161, 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	GPR161, RPL21P27, 238 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	GPR161, LOC100420658, 167 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	GPR161, 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	GPR161, ATP1B1, 156 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 34

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Number of Variants: 20

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Supplemental Content

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