slc38a8[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
nsv7095050	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,050,104-84,050,912 , GRCh38.p12 chr16: 84,016,499-84,017,307	SLC38A8
nsv7094697	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 84,043,389-84,043,502 , GRCh38.p12 chr16: 84,009,784-84,009,897	SLC38A8
nsv6310098	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 83,932,750-84,056,514 , GRCh38.p12 chr16: 83,899,145-84,022,909	SLC38A8, MLYCD, 3 more genes
nsv3901167	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 83,935,523-84,057,571 , GRCh38.p12 chr16: 83,901,918-84,023,966	SLC38A8, MLYCD, 3 more genes
nsv3902255	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 84,048,416-84,125,270 , GRCh38.p12 chr16: 84,014,811-84,091,665	SLC38A8, MBTPS1, 1 more genes
nsv3900416	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 84,053,035-84,120,718 , GRCh38.p12 chr16: 84,019,430-84,087,113	SLC38A8, MBTPS1, 1 more genes
nsv4456540	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 83,904,100-84,058,759 , GRCh38.p12 chr16: 83,870,495-84,025,154	SLC38A8, MLYCD, 3 more genes
nsv4675079	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 83,903,257-84,057,905 , GRCh38.p12 chr16: 83,869,652-84,024,300	SLC38A8, NECAB2, 3 more genes
nsv4456321	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 83,970,585-84,077,491 , GRCh38.p12 chr16: 83,936,980-84,043,886	SLC38A8, RNA5SP432, 2 more genes
nsv3893906	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 84,064,488-84,118,876 , GRCh38.p12 chr16: 84,030,883-84,085,271	SLC38A8, RNA5SP432, 1 more genes
nsv7095104	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 84,046,586-84,126,922 , GRCh38.p12 chr16: 84,012,981-84,093,317	SLC38A8, MBTPS1, 1 more genes
nsv4455803	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 84,046,463-84,126,358 , GRCh38.p12 chr16: 84,012,858-84,092,753	SLC38A8, MBTPS1, 1 more genes
nsv5673088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,005,756-84,164,926 , GRCh38.p12 chr16: 83,972,151-84,131,321	SLC38A8, MBTPS1, 4 more genes
nsv3921095	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726	SLC38A8, NECAB2, 219 more genes
nsv3919844	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,704,275-87,819,342 , GRCh37 chr16: 78,738,172-87,852,948 , NCBI36 chr16: 77,295,673-86,410,449	SLC38A8, RPL10AP12, 146 more genes
nsv3917609	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 80,344,868-84,305,898 , GRCh37 chr16: 81,787,367-85,748,397 , GRCh38 chr16: 81,753,762-85,714,791	SLC38A8, LOC105371376, 63 more genes
nsv3911104	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 83,912,597-87,257,444 , GRCh38 chr16: 83,878,992-87,223,838 , NCBI36 chr16: 82,470,098-85,814,945	SLC38A8, LOC101928557, 75 more genes
nsv3922440	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 82,278,756-84,664,347 , GRCh37 chr16: 83,721,255-86,106,846 , GRCh38 chr16: 83,687,650-86,073,240	SLC38A8, LOC123862, 58 more genes
nsv3922490	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 83,016,872-85,087,809 , GRCh37 chr16: 83,050,477-85,121,415 , NCBI36 chr16: 81,607,978-83,678,916	SLC38A8, MBTPS1, 33 more genes
nsv3922339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 83,432,665-84,941,726 , GRCh38 chr16: 83,399,060-84,908,120 , NCBI36 chr16: 81,990,166-83,499,227	SLC38A8, LOC648774, 28 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 90

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Number of Variants: 20

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