osbpl2[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7096265	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 60,854,193-60,886,170 , GRCh38.p12 chr20: 62,279,137-62,311,114	OSBPL2, LAMA5, 1 more genes
nsv7095800	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 60,861,619-60,890,283 , GRCh38.p12 chr20: 62,286,563-62,315,227	OSBPL2, ADRM1, 1 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, 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	OSBPL2, GID8, 204 more genes
nsv4676332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636	OSBPL2, BMP7, 153 more genes
nsv6314208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,835,739-62,915,555 , GRCh38.p12 chr20: 58,260,683-64,284,202	OSBPL2, LOC105372698, 176 more genes
nsv4676181	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052	OSBPL2, LOC105372697, 174 more genes
nsv3916789	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118	OSBPL2, RNU7-141P, 153 more genes
nsv3924353	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679	OSBPL2, PPDPF, 126 more genes
nsv3896614	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 60,053,234-62,961,294 , GRCh38.p12 chr20: 61,478,178-64,329,941	OSBPL2, TNFRSF6B, 128 more genes
nsv3895755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 60,063,645-62,961,294 , GRCh38.p12 chr20: 61,488,589-64,329,941	OSBPL2, LOC105372717, 128 more genes
nsv3894116	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202	OSBPL2, ATP5F1E, 254 more genes

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

Send to:

Search results

Items: 1 to 20 of 30

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 30

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity