kif11[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
nsv7093814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,388,545-94,413,553 , GRCh38.p12 chr10: 92,628,788-92,653,796	KIF11
nsv6309173	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,392,223-94,393,572 , GRCh38.p12 chr10: 92,632,466-92,633,815	KIF11
nsv7093813	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,372,777-94,373,396 , GRCh38.p12 chr10: 92,613,020-92,613,639	KIF11
nsv4454339	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 92,609,020-92,609,509 , GRCh37 chr10: 94,368,777-94,369,266	KIF11
nsv5672768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,405,120-94,405,399 , GRCh38.p12 chr10: 92,645,363-92,645,642	KIF11
nsv7093899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,366,896-94,367,014 , GRCh38.p12 chr10: 92,607,139-92,607,257	KIF11
nsv7093812	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,353,133-94,353,229 , GRCh38.p12 chr10: 92,593,376-92,593,472	KIF11
nsv7093658	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 94,362,577-94,366,140 , GRCh38.p12 chr10: 92,602,820-92,606,383	KIF11
nsv6309090	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 94,368,757-94,405,419 , GRCh38.p12 chr10: 92,609,000-92,645,662	KIF11
nsv4683660	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 94,381,142-94,405,399 , GRCh38.p12 chr10: 92,621,385-92,645,642	KIF11
nsv6314450	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr10: 92,621,486-92,621,486 , GRCh37 chr10: 94,381,243-94,381,243	KIF11
nsv7093657	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 94,353,133-94,405,419 , GRCh38.p12 chr10: 92,593,376-92,645,662	KIF11, RPL11P4
nsv997243	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr10: 92,593,068-92,655,395 , GRCh37 chr10: 94,352,825-94,415,152	KIF11, RPL11P4
nsv1398191	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 94,368,870-94,715,405 , GRCh38.p12 chr10: 92,609,113-92,955,648	KIF11, HHEX, 3 more genes
nsv4682413	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 94,243,012-94,392,450 , GRCh38.p12 chr10: 92,483,255-92,632,693	KIF11, RPL11P4, 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	KIF11, RNU7-12P, 1876 more genes
nsv3920295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422	KIF11, EIF2S2P3, 895 more genes
nsv3894877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966	KIF11, RNY3P12, 146 more genes
nsv3908115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627	KIF11, EXOC6, 118 more genes
nsv6637868	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184	KIF11, RPS27P1, 118 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 34

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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