tmx1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916278	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390	TMX1, LOC105370507, 98 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	TMX1, 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	TMX1, 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	TMX1, 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	TMX1, 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	TMX1, 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	TMX1, 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	TMX1, 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	TMX1, PAPOLA-DT, 1338 more genes
nsv3911849	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461	TMX1, ARF6, 219 more genes
nsv3911178	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 49,627,618-51,313,793 , GRCh37 chr14: 50,557,868-52,244,043 , GRCh38 chr14: 50,091,150-51,777,325	TMX1, TRIM9, 35 more genes
nsv3903380	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 50,598,842-52,261,074 , GRCh38.p12 chr14: 50,132,124-51,794,356	TMX1, LINC02310, 33 more genes
nsv4456410	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 51,357,592-51,951,601 , GRCh38.p12 chr14: 50,890,874-51,484,883	TMX1, LOC400212, 10 more genes

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tmx1[All Fields] AND 1[has_clinical] (14)
dbVar
Taxonomy Links for Nucleotide (Select 2048728470) (1)
Taxonomy
katanin-interacting protein isoform X13 [Homo sapiens]
katanin-interacting protein isoform X13 [Homo sapiens]
gi|2217305244|ref|XP_047289800.1|

Protein
protein monoglycylase TTLL8 isoform X5 [Homo sapiens]
protein monoglycylase TTLL8 isoform X5 [Homo sapiens]
gi|2462584027|ref|XP_054181192.1|

Protein

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