osgin1[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
nsv3905548	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 83,998,698-84,024,074 , GRCh38.p12 chr16: 83,965,093-83,990,469	OSGIN1, NECAB2
nsv3908578	copy number variation	1	nstd102	human	Benign/Likely benign	GRCh37 chr16: 83,986,845-84,014,686 , GRCh38.p12 chr16: 83,953,240-83,981,081	OSGIN1, NECAB2
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	OSGIN1, 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	OSGIN1, MLYCD, 3 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, SLC38A8, 2 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, 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	OSGIN1, LOC648774, 28 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	OSGIN1, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	OSGIN1, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	OSGIN1, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	OSGIN1, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	OSGIN1, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	OSGIN1, LOC105371237, 985 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 81

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Number of Variants: 20

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