mark3[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
nsv3895071	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 103,850,963-103,878,882 , GRCh38.p12 chr14: 103,384,626-103,412,545	MARK3, RPL10AP1
nsv3914561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 95,990,744-107,287,708 , GRCh38 chr14: 95,524,407-106,879,501 , NCBI36 chr14: 95,060,497-106,358,753	MARK3, MIR889, 517 more genes
nsv4684265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456	MARK3, NDUFB3P4, 502 more genes
nsv3911746	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 97,938,637-106,855,263 , GRCh37 chr14: 98,404,974-107,263,478 , NCBI36 chr14: 97,474,727-106,334,523	MARK3, MIR1185-2, 477 more genes
nsv3921506	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 99,831,655-106,855,263 , GRCh37 chr14: 100,297,992-107,263,478 , NCBI36 chr14: 99,367,745-106,334,523	MARK3, RPL21P13, 453 more genes
nsv3902723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 100,661,319-107,285,437 , GRCh38.p12 chr14: 100,194,982-106,877,229	MARK3, NDUFB3P4, 448 more genes
nsv3922827	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 100,309,382-106,855,263 , GRCh37 chr14: 100,775,719-107,263,478 , NCBI36 chr14: 99,845,472-106,334,523	MARK3, RNU6-1316P, 440 more genes
nsv3914191	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 100,118,149-106,356,482 , GRCh38 chr14: 100,582,059-106,877,229 , GRCh37 chr14: 101,048,396-107,285,437	MARK3, IGHV4-55, 436 more genes
nsv3918080	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 100,344,390-106,334,523 , GRCh37 chr14: 101,274,637-107,263,478 , GRCh38 chr14: 100,808,300-106,855,263	MARK3, GPR132, 427 more genes
nsv6314048	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,732,158-107,285,437 , GRCh38.p12 chr14: 101,265,821-106,877,229	MARK3, IGHD4-23, 329 more genes
nsv4456944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681	MARK3, IGHV1-58, 308 more genes
nsv3917997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,131,939-107,263,478 , NCBI36 chr14: 101,201,692-106,334,523 , GRCh38 chr14: 101,665,602-106,855,263	MARK3, IGHV3-23, 315 more genes
nsv3917679	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 101,925,670-106,876,323 , GRCh37 chr14: 102,392,007-107,284,531 , NCBI36 chr14: 101,461,760-106,355,576	MARK3, LINC00221, 313 more genes
nsv4729218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229	MARK3, IGHV4-61, 308 more genes
nsv3893817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,670,706-107,285,437 , GRCh38.p12 chr14: 102,204,369-106,877,229	MARK3, MOK, 308 more genes
nsv3914922	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 102,239,422-106,877,229 , GRCh37 chr14: 102,705,759-107,285,437 , NCBI36 chr14: 101,775,512-106,356,482	MARK3, GPR132, 306 more genes
nsv7148227	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 102,263,440-106,874,929 , GRCh37.p13 chr14: 102,729,777-107,283,138	MARK3, TNFAIP2, 306 more genes
nsv6291499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 101,593,860-106,160,500 , GRCh38.p12 chr14: 101,127,523-105,605,042	MARK3, CDC42BPB, 133 more genes
nsv4456320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229	MARK3, LOC105378184, 302 more genes
nsv3918299	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 102,605,096-106,879,298 , GRCh37 chr14: 103,071,433-107,287,505 , NCBI36 chr14: 102,141,186-106,358,550	MARK3, IGHVII-30-1, 295 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 59

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Number of Variants: 20

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Supplemental Content

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Search details

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