slc38a6[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
nsv7094258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 61,441,827-61,447,691 , GRCh38.p12 chr14: 60,975,109-60,980,973	SLC38A6, TRMT5
nsv7094440	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 61,444,212-61,447,691 , GRCh38.p12 chr14: 60,977,494-60,980,973	SLC38A6, TRMT5
nsv7093469	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr14: 60,979,574-60,979,574 , GRCh37 chr14: 61,446,292-61,446,292	SLC38A6, TRMT5
nsv4675800	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr14: 61,409,856-61,547,332 , GRCh38.p12 chr14: 60,943,138-61,080,614	SLC38A6, RNU6-398P, 3 more genes
nsv3891628	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 61,347,538-61,453,942 , GRCh38.p12 chr14: 60,880,820-60,987,224	SLC38A6, RNU6-398P, 3 more genes
nsv4456519	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 61,393,999-61,520,353 , GRCh38.p12 chr14: 60,927,281-61,053,635	SLC38A6, MNAT1, 3 more genes
nsv3922652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231	SLC38A6, PARP1P2, 160 more genes
nsv3923965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803	SLC38A6, ESR2, 111 more genes
nsv3924033	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999	SLC38A6, DACT1, 105 more genes
nsv3915521	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 57,682,493-60,810,090 , GRCh37 chr14: 58,612,740-61,740,337 , GRCh38 chr14: 58,146,022-61,273,619	SLC38A6, DACT1, 61 more genes
nsv3910126	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 58,143,026-61,052,791 , GRCh37.p13 chr14: 59,073,273-61,983,038 , GRCh38.p12 chr14: 58,606,555-61,516,320	SLC38A6, AKR1B1P5, 45 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, 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	SLC38A6, PAPOLA-DT, 1338 more genes
nsv6637682	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485	SLC38A6, PARP1P2, 91 more genes

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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 26

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Number of Variants: 20

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