med6[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3923727	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 70,028,816-82,441,728 , GRCh38 chr14: 69,562,099-81,975,384 , NCBI36 chr14: 69,098,569-81,511,481	MED6, CEP128, 240 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	MED6, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	MED6, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	MED6, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	MED6, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	MED6, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	MED6, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	MED6, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	MED6, PAPOLA-DT, 1338 more genes
nsv3903706	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 68,035,240-73,568,130 , GRCh38.p12 chr14: 67,568,523-73,101,422	MED6, ACTN1, 108 more genes
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	MED6, ACTN1, 400 more genes
nsv3903413	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 71,040,157-71,240,681 , GRCh38.p12 chr14: 70,573,440-70,773,964	MED6, LINC01269, 6 more genes

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med6[All Fields] AND 1[has_clinical] (13)
dbVar
SOX5[gene] (300)
ClinVar
ETV6[gene] (409)
ClinVar
hypothetical protein FA954_03245 [Thermoactinomyces vulgaris]
hypothetical protein FA954_03245 [Thermoactinomyces vulgaris]
gi|1672833107|gnl|PRJNA534300|FA954 5|gb|QCV54713.1|

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