pot1[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
nsv4454827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 124,823,952-124,897,183 , GRCh37 chr7: 124,464,006-124,537,237	POT1
nsv7097478	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr7: 124,464,016-124,537,227 , GRCh38.p12 chr7: 124,823,962-124,897,173	POT1
nsv5564495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,486,986-124,537,227 , GRCh38.p12 chr7: 124,846,932-124,897,173	POT1
nsv7097861	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,491,926-124,537,227 , GRCh38.p12 chr7: 124,851,872-124,897,173	POT1
nsv7097479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,503,394-124,537,227 , GRCh38.p12 chr7: 124,863,340-124,897,173	POT1
nsv5381541	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,510,955-124,537,227 , GRCh38.p12 chr7: 124,870,901-124,897,173	POT1
nsv4682136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,481,017-124,493,202 , GRCh38.p12 chr7: 124,840,963-124,853,148	POT1
nsv5381634	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,499,001-124,511,105 , GRCh38.p12 chr7: 124,858,947-124,871,051	POT1
nsv3883956	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 124,852,966-124,853,144 , GRCh37 chr7: 124,493,020-124,493,198	POT1
nsv5381632	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,482,851-124,483,027 , GRCh38.p12 chr7: 124,842,797-124,842,973	POT1
nsv4682669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,532,310-124,532,444 , GRCh38.p12 chr7: 124,892,256-124,892,390	POT1
nsv6312523	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 124,475,323-124,475,478 , GRCh38.p12 chr7: 124,835,269-124,835,424	POT1
nsv3879041	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 124,870,905-124,897,179 , GRCh37.p13 chr7: 124,510,959-124,537,233	POT1
nsv4681163	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,481,017-124,483,027 , GRCh38.p12 chr7: 124,840,963-124,842,973	POT1
nsv7097860	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,464,016-124,465,421 , GRCh38.p12 chr7: 124,823,962-124,825,367	POT1
nsv4683857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,503,394-124,503,704 , GRCh38.p12 chr7: 124,863,340-124,863,650	POT1
nsv4681477	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,486,986-124,487,062 , GRCh38.p12 chr7: 124,846,932-124,847,008	POT1
nsv4681054	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,475,323-124,537,237 , GRCh38.p12 chr7: 124,835,269-124,897,183	POT1
nsv4682880	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,464,006-124,511,105 , GRCh38.p12 chr7: 124,823,952-124,871,051	POT1
nsv6312612	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 124,464,016-124,511,105 , GRCh38.p12 chr7: 124,823,962-124,871,051	POT1

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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 56

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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