tnr[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
nsv7097105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,120,137-117,173,634 , GRCh38.p12 chr7: 117,480,083-117,533,580	CFTR
nsv4436263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,254,667-117,307,162 , GRCh38 chr7: 117,614,613-117,667,108	CFTR
nsv6290193	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,120,202-117,170,952 , GRCh38.p12 chr7: 117,480,148-117,530,898	CFTR
nsv5673930	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,218,381-117,254,777 , GRCh38.p12 chr7: 117,578,327-117,614,723	CFTR
nsv7098785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,120,202-117,149,087 , GRCh38.p12 chr7: 117,480,148-117,509,033	CFTR
nsv4683481	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,227,774-117,254,777 , GRCh38.p12 chr7: 117,587,720-117,614,723	CFTR
nsv4682799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,144,294-117,171,255 , GRCh38.p12 chr7: 117,504,240-117,531,201	CFTR
nsv6312520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,266,272-117,292,995 , GRCh38.p12 chr7: 117,626,218-117,652,941	CFTR
nsv3883463	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,138,363-117,159,446 , GRCh38 chr7: 117,498,309-117,519,392	CFTR
nsv3870481	copy number variation	4	nstd102	human	Pathogenic, not provided	GRCh37 chr7: 117,138,367-117,159,446 , GRCh38 chr7: 117,498,313-117,519,392	CFTR
nsv4728450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,246,808-117,267,575 , GRCh38.p12 chr7: 117,606,754-117,627,521	CFTR
nsv4456907	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,141,921-117,159,386 , GRCh38.p12 chr7: 117,501,867-117,519,332	CFTR
nsv7136990	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,292,986-117,306,961 , GRCh38.p12 chr7: 117,652,932-117,666,907	CFTR
nsv6289866	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 117,652,853-117,666,141 , GRCh37.p13 chr7: 117,292,907-117,306,195	CFTR
nsv6137757	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 117,602,152-117,612,040 , GRCh37 chr7: 117,242,206-117,252,094	CFTR
nsv4681809	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,242,783-117,251,882 , GRCh38.p12 chr7: 117,602,729-117,611,828	CFTR
nsv4683598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,242,847-117,251,872 , GRCh38.p12 chr7: 117,602,793-117,611,818	CFTR
nsv5059992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,244,921-117,252,122 , GRCh38 chr7: 117,604,867-117,612,068	CFTR
nsv4769264	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,264,692-117,269,970 , GRCh38 chr7: 117,624,638-117,629,916	CFTR
nsv5673842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 117,246,713-117,251,872 , GRCh38.p12 chr7: 117,606,659-117,611,818	CFTR

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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 189

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Number of Variants: 20

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Supplemental Content

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Search details

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