kif2a[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
nsv3880606	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 61,574,836-61,606,371 , GRCh38.p12 chr5: 62,279,009-62,310,544	KIF2A
nsv3883529	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 61,574,991-61,600,316 , GRCh38.p12 chr5: 62,279,164-62,304,489	KIF2A
nsv6312112	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 61,602,300-61,602,383 , GRCh38.p12 chr5: 62,306,473-62,306,556	KIF2A
nsv6312113	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 61,602,300-61,662,328 , GRCh38.p12 chr5: 62,306,473-62,366,501	KIF2A, LOC100421358
nsv7096780	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 61,642,937-61,681,396 , GRCh38.p12 chr5: 62,347,110-62,385,569	KIF2A, DIMT1
nsv7096781	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 61,653,944-61,681,396 , GRCh38.p12 chr5: 62,358,117-62,385,569	KIF2A, DIMT1
nsv6312205	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr5: 61,602,300-61,681,396 , GRCh38.p12 chr5: 62,306,473-62,385,569	KIF2A, LOC100421358, 1 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	KIF2A, MEGF10, 2080 more genes
nsv3923429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770	KIF2A, ISCA1P1, 163 more genes
nsv6315417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 59,783,655-63,257,950 , GRCh38.p12 chr5: 60,487,828-63,962,123	KIF2A, ERCC8, 41 more genes
nsv3919086	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 59,830,661-63,259,366 , GRCh38 chr5: 60,499,077-63,927,783 , GRCh37 chr5: 59,794,904-63,223,610	KIF2A, LOC105378999, 40 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	KIF2A, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	KIF2A, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	KIF2A, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	KIF2A, LINC02241, 878 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	KIF2A, TRIM23, 215 more genes
nsv3883692	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239	KIF2A, TRIM23, 125 more genes
nsv3880956	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 61,535,404-61,926,784 , GRCh38.p12 chr5: 62,239,577-62,630,957	KIF2A, CKS1BP3, 7 more genes
nsv3884687	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 61,618,595-61,811,970 , GRCh38.p12 chr5: 62,322,768-62,516,143	KIF2A, DIMT1, 4 more genes
nsv4676090	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 61,432,724-62,050,314 , GRCh38.p12 chr5: 62,136,897-62,754,487	KIF2A, IPO11-LRRC70, 9 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 29

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Number of Variants: 20

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Supplemental Content

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