ogfr[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
nsv3896552	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 61,441,901-61,458,171 , GRCh38.p12 chr20: 62,810,549-62,826,819	OGFR, COL9A3
nsv6314131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202	OGFR, HAR1A, 100 more genes
nsv4676208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202	OGFR, GMEB2, 94 more genes
nsv3916163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,211,869-62,908,674 , GRCh38 chr20: 62,561,794-64,277,321 , NCBI36 chr20: 60,569,446-62,379,118	OGFR, LOC105372727, 94 more genes
nsv3916631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,179,280-62,915,555 , NCBI36 chr20: 60,589,725-62,385,999 , GRCh38 chr20: 62,582,073-64,284,202	OGFR, PTK6, 91 more genes
nsv3922590	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839	OGFR, RPL7P3, 95 more genes
nsv3913089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,765,104-62,385,999 , GRCh37 chr20: 61,294,659-62,915,555 , GRCh38 chr20: 62,663,307-64,284,202	OGFR, SLCO4A1-AS1, 89 more genes
nsv3911578	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,455,231-63,839,491 , NCBI36 chr20: 60,463,682-61,941,288 , GRCh37 chr20: 61,030,287-62,470,844	OGFR, LOC105372716, 70 more genes
nsv7148178	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 62,632,017-63,794,804 , GRCh37.p13 chr20: 61,267,734-62,426,157	OGFR, GID8, 60 more genes
nsv3903709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,429,900-62,293,991 , GRCh38.p12 chr20: 62,798,548-63,662,638	OGFR, RNU6-994P, 48 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	OGFR, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	OGFR, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	OGFR, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	OGFR, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	OGFR, MIR3646, 1310 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	OGFR, FTLP1, 472 more genes
nsv6112778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273	OGFR, LINC01742, 253 more genes
nsv3911673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321	OGFR, LOC105372709, 226 more genes
nsv4357849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528	OGFR, RBM38, 192 more genes
nsv3910216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,804,471-62,904,442 , NCBI36 chr20: 55,237,878-62,374,886 , GRCh38 chr20: 57,229,415-64,273,089	OGFR, GID8, 204 more genes

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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 50

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Number of Variants: 20

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Supplemental Content

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