gc[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
nsv4682160	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 791,895-795,026 , GRCh38.p12 chr11: 791,895-795,026	SLC25A22
nsv3905175	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 106,771,576-106,805,698 , GRCh38.p12 chr11: 106,900,850-106,934,972	GUCY1A2
nsv3896651	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 106,780,118-106,805,698 , GRCh38.p12 chr11: 106,909,392-106,934,972	GUCY1A2
nsv3901529	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 106,780,730-106,805,698 , GRCh38.p12 chr11: 106,910,004-106,934,972	GUCY1A2
nsv3898695	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 106,786,428-106,808,500 , GRCh38.p12 chr11: 106,915,702-106,937,774	GUCY1A2
nsv3873595	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 156,587,886-156,598,081 , GRCh38.p12 chr4: 155,666,734-155,676,929	GUCY1A1
nsv3889886	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 156,587,887-156,598,081 , GRCh38.p12 chr4: 155,666,735-155,676,929	GUCY1A1
nsv3900352	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 106,786,428-106,789,492 , GRCh38.p12 chr11: 106,915,702-106,918,766	GUCY1A2
nsv3881172	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 156,595,742-156,598,385 , GRCh38.p12 chr4: 155,674,590-155,677,233	GUCY1A1
nsv3875994	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 156,596,190-156,598,385 , GRCh38.p12 chr4: 155,675,038-155,677,233	GUCY1A1
nsv3888732	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 108,231,394-108,656,588 , GRCh38.p12 chrX: 108,988,164-109,413,359	GUCY2F
nsv6309747	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,478,555-91,479,232 , GRCh38.p12 chr15: 90,935,325-90,936,002	UNC45A
nsv7094746	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,488,102-91,488,313 , GRCh38.p12 chr15: 90,944,872-90,945,083	UNC45A
nsv7094797	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,478,555-91,486,332 , GRCh38.p12 chr15: 90,935,325-90,943,102	UNC45A
nsv7097239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 156,618,020-156,651,383 , GRCh38.p12 chr4: 155,696,868-155,730,231	GUCY1A1, LOC105377506
nsv4685996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 35,799,615-35,808,850 , GRCh38.p12 chr9: 35,799,618-35,808,853	NPR2, SPAG8
nsv3893360	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 7,107,939-7,136,456 , GRCh38.p12 chr11: 7,086,708-7,115,225	RBMXL2, NLRP14
nsv6313669	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 72,609,397-72,873,579 , GRCh38.p12 chr4: 71,743,680-72,007,862	GC, RNA5SP163
nsv7094317	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 91,489,824-91,496,946 , GRCh38.p12 chr15: 90,946,594-90,953,716	UNC45A, RCCD1
nsv6309474	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 14,832,571-14,839,179 , GRCh38.p12 chr12: 14,679,637-14,686,245	GUCY2C, C12orf60

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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 720

Page of 36

Number of Variants: 20

Page of 36

Supplemental Content

Find related data

Search details

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