cabcoco1[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
nsv3920758	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 63,153,647-63,439,111 , GRCh37 chr10: 63,483,641-63,769,105 , GRCh38 chr10: 61,723,883-62,009,346	CABCOCO1, LINC02625, 1 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	CABCOCO1, RNU7-12P, 1876 more genes
nsv4675455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325	CABCOCO1, MRLN, 242 more genes
nsv3922335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980	CABCOCO1, UNC5B-AS1, 250 more genes
nsv4675436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638	CABCOCO1, MRPL35P2, 77 more genes
nsv4675795	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 55,589,950-63,990,649 , GRCh38.p12 chr10: 53,830,190-62,230,890	CABCOCO1, ARL4AP1, 52 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	CABCOCO1, LOC100419870, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	CABCOCO1, AGAP14P, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	CABCOCO1, ANXA11, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	CABCOCO1, TUBB8, 2085 more genes
nsv7137211	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639	CABCOCO1, EXOC6, 1906 more genes
nsv3924859	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961	CABCOCO1, BMS1P4-AGAP5, 471 more genes
nsv3917047	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908	CABCOCO1, SLC9A3P3, 476 more genes
nsv3921181	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 41,927,641-68,830,439 , GRCh38 chr10: 42,112,187-67,400,675 , GRCh37 chr10: 42,607,635-69,160,433	CABCOCO1, AGAP6, 338 more genes
nsv3919727	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 55,287,177-67,558,442 , GRCh37 chr10: 57,046,937-69,318,200 , NCBI36 chr10: 56,716,943-68,988,206	CABCOCO1, RNU6-543P, 96 more genes
nsv3905569	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 57,587,928-64,212,007 , GRCh38.p12 chr10: 55,828,168-62,452,248	CABCOCO1, ANK3, 48 more genes
nsv3907664	copy number variation	1	nstd102	human	drug response	GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422	CABCOCO1, SHOC2, 1487 more genes
nsv6637363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 57,941,252-64,846,332 , GRCh38.p12 chr10: 56,181,491-63,086,572	CABCOCO1, TMEM26-AS1, 53 more genes
nsv4674969	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 62,191,184-65,348,431 , GRCh38.p12 chr10: 60,431,426-63,588,671	CABCOCO1, RNU6-543P, 33 more genes
nsv6637322	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 60,870,153-63,790,451 , GRCh38.p12 chr10: 59,110,393-62,030,692	CABCOCO1, MRPL50P4, 25 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 22

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 22

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity