rrp7a[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
nsv3908963	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 42,912,097-42,952,466 , GRCh38.p12 chr22: 42,516,091-42,556,460	RRP7A, SERHL2
nsv3890491	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 42,912,722-42,952,466 , GRCh38.p12 chr22: 42,516,716-42,556,460	RRP7A, SERHL2
nsv3900965	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 42,879,503-42,952,466 , GRCh38.p12 chr22: 42,483,497-42,556,460	RRP7A, SERHL, 2 more genes
nsv3898735	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 42,880,070-42,946,371 , GRCh38.p12 chr22: 42,484,064-42,550,365	RRP7A, LOC101927372, 1 more genes
nsv3922269	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr22: 41,101,021-41,237,734 , GRCh37.p13 chr22: 42,771,077-42,907,790 , GRCh38.p12 chr22: 42,375,071-42,511,784	RRP7A, LOC101927344, 3 more genes
nsv3900214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300	RRP7A, TYMP, 218 more genes
nsv6290298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638	RRP7A, CERK, 212 more genes
nsv3912011	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264	RRP7A, TUBGCP6, 213 more genes
nsv5381149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300	RRP7A, WBP2NL, 210 more genes
nsv4351202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331	RRP7A, PLXNB2, 204 more genes
nsv3893572	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410	RRP7A, CYP2D8P, 206 more genes
nsv3920027	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 42,433,752-50,738,932 , NCBI36 chr22: 41,159,702-49,524,226 , GRCh37 chr22: 42,829,758-51,177,360	RRP7A, MIR6821, 187 more genes
nsv3923135	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 42,493,445-50,268,479 , GRCh37 chr22: 42,889,451-50,706,908 , NCBI36 chr22: 41,219,395-49,049,035	RRP7A, LINC01656, 156 more genes
nsv5673276	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994	RRP7A, RPL5P34, 48 more genes
nsv5381088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996	RRP7A, CYP2D8P, 49 more genes
nsv7096314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,456,283-43,089,957 , GRCh38.p12 chr22: 42,060,279-42,693,951	RRP7A, SERHL2, 28 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	RRP7A, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	RRP7A, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	RRP7A, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	RRP7A, FBXO7, 1084 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

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Items: 1 to 20 of 46

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Number of Variants: 20

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