kremen1[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
nsv3923205	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926	KREMEN1, DRG1, 138 more genes
nsv3924941	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 26,221,273-29,477,543 , GRCh37 chr22: 26,617,239-29,873,532 , NCBI36 chr22: 24,947,239-28,203,532	KREMEN1, TFIP11, 66 more genes
nsv6637977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 26,614,429-29,847,680 , GRCh38.p12 chr22: 26,218,463-29,451,691	KREMEN1, MIAT, 65 more genes
nsv4729897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 28,291,202-30,450,920 , GRCh38.p12 chr22: 27,895,214-30,054,931	KREMEN1, RNU6-810P, 48 more genes
nsv3918839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 28,837,023-30,672,500 , GRCh38 chr22: 28,441,035-30,276,511 , NCBI36 chr22: 27,167,023-29,002,500	KREMEN1, RPEP4, 51 more genes
nsv5673427	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,083,885-30,337,586 , GRCh38.p12 chr22: 28,687,897-29,941,597	KREMEN1, SNORD125, 36 more genes
nsv5673351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,105,984-30,337,586 , GRCh38.p12 chr22: 28,709,996-29,941,597	KREMEN1, SNORD125, 36 more genes
nsv4683866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,083,875-30,090,801 , GRCh38.p12 chr22: 28,687,887-29,694,812	KREMEN1, RNU6-1219P, 29 more genes
nsv3918005	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,252,132-29,902,266 , NCBI36 chr22: 27,582,132-28,232,266 , GRCh38 chr22: 28,856,144-29,506,277	KREMEN1, AP1B1, 20 more genes
nsv4682263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 29,083,885-29,621,477 , GRCh38.p12 chr22: 28,687,897-29,225,488	KREMEN1, XBP1, 13 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	KREMEN1, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	KREMEN1, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	KREMEN1, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	KREMEN1, FBXO7, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	KREMEN1, FABP5P11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	KREMEN1, DDTL, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	KREMEN1, YPEL1, 1083 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	KREMEN1, IGLV3-27, 1082 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	KREMEN1, POM121L7P, 1082 more genes
nsv3913775	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264	KREMEN1, ZNF280A, 1059 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 31

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Number of Variants: 20

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Supplemental Content

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Search details

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