znf365[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
nsv3922725	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr10: 63,814,805-64,014,880 , GRCh38 chr10: 62,385,040-62,585,115 , GRCh37 chr10: 64,144,799-64,344,874	ZNF365
nsv3916665	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 63,675,820-63,814,790 , GRCh37.p13 chr10: 64,005,814-64,144,784 , GRCh38.p12 chr10: 62,246,055-62,385,025	ZNF365, RN7SL591P, 3 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, MRPL35P2, 77 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, 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	ZNF365, RNU6-543P, 33 more genes
nsv3921516	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr10: 60,977,777-62,913,465 , NCBI36 chr10: 62,407,541-64,343,231 , GRCh37 chr10: 62,737,535-64,673,225	ZNF365, LOC283045, 16 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 21

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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