kif5c[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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	KIF5C, DAZAP2P1, 2991 more genes
nsv3898306	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 148,917,286-163,204,623 , GRCh37 chr2: 149,674,855-164,061,133 , NCBI36 chr2: 149,391,325-163,769,379	KIF5C, RPS3AP13, 170 more genes
nsv4674226	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 147,173,792-158,346,266 , GRCh38.p12 chr2: 146,416,224-157,489,754	KIF5C, RBM43, 120 more genes
nsv3902718	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 147,251,948-157,856,378 , NCBI36 chr2: 147,725,986-158,421,136 , GRCh37 chr2: 148,009,516-158,712,890	KIF5C, RNU6-1275P, 117 more genes
nsv6313481	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305	KIF5C, STIP1P1, 98 more genes
nsv3903939	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,347,892-154,353,187 , NCBI36 chr2: 148,064,362-154,061,433 , GRCh38 chr2: 147,590,324-153,496,674	KIF5C, MIR4773-2, 68 more genes
nsv3878148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 146,913,477-151,531,586 , GRCh38.p12 chr2: 146,155,909-150,675,072	KIF5C, LINC01911, 48 more genes
nsv3901591	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 145,471,053-149,582,570 , NCBI36 chr2: 145,945,091-150,147,330 , GRCh37 chr2: 146,228,621-150,439,084	KIF5C, TXNP5, 41 more genes
nsv3885378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,842,506-152,370,040 , GRCh38.p12 chr2: 148,084,937-151,513,526	KIF5C, LINC01931, 45 more genes
nsv1398486	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 146,798,229-150,310,317 , GRCh37.p13 chr2: 147,081,759-150,602,071 , GRCh38.p12 chr2: 146,324,191-149,745,557	KIF5C, LINC01911, 38 more genes
nsv1398418	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 148,447,496-149,377,297 , GRCh38 chr2: 147,973,457-148,903,258 , GRCh37 chr2: 148,731,026-149,660,827	KIF5C, USP12P2, 14 more genes
nsv3909847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 149,198,443-149,948,302 , GRCh38 chr2: 148,440,874-149,091,788 , NCBI36 chr2: 148,914,913-149,656,548	KIF5C, LOC101928553, 11 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	KIF5C, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	KIF5C, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	KIF5C, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	KIF5C, MTND2P22, 3724 more genes
nsv5381338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882	KIF5C, YY1P2, 156 more genes
nsv3904897	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 143,900,149-158,321,624 , GRCh37 chr2: 144,657,717-159,178,136 , NCBI36 chr2: 144,374,187-158,886,382	KIF5C, RPLP0P7, 149 more genes
nsv6290982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 142,409,401-152,680,804 , GRCh38.p12 chr2: 141,651,832-151,824,290	KIF5C, LOC101928526, 101 more genes
nsv3906056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 147,081,759-157,075,637 , NCBI36 chr2: 146,798,229-156,783,883 , GRCh38 chr2: 146,324,191-156,219,125	KIF5C, LOC105373698, 104 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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Search details

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