6[Chr] AND (1500000:3000000[ChrPos] OR 1500000:3000000[ChrEnd]) - 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
nsv3882358	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 1,610,446-1,613,897 , GRCh37 chr6: 1,610,681-1,614,132	FOXC1
nsv3879099	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 1,610,426-1,612,841 , GRCh37 chr6: 1,610,661-1,613,076	FOXC1
nsv3877237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 1,610,445-1,612,107 , GRCh37 chr6: 1,610,680-1,612,342	FOXC1
nsv7097816	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 1,609,367-1,610,939 , GRCh38.p12 chr6: 1,609,132-1,610,704	FOXC1
nsv7097052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 1,610,666-1,612,017 , GRCh38.p12 chr6: 1,610,431-1,611,782	FOXC1
nsv997060	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr6: 1,610,446-1,613,897 , GRCh37 chr6: 1,610,681-1,614,132	FOXC1
nsv6312470	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr6: 1,610,681-1,612,342 , GRCh38.p12 chr6: 1,610,446-1,612,107	FOXC1
nsv7093107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 1,611,469-1,611,470 , GRCh38 chr6: 1,611,234-1,611,235	FOXC1
nsv3877090	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 1,703,078-1,918,006 , GRCh38.p12 chr6: 1,702,844-1,917,772	GMDS
nsv3883034	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 2,207,469-2,208,093 , GRCh38.p12 chr6: 2,207,235-2,207,859	GMDS
nsv3889911	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 2,207,469-2,208,008 , GRCh38.p12 chr6: 2,207,235-2,207,774	GMDS
nsv3910310	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,744,238-2,006,788 , NCBI36 chr6: 1,689,237-1,951,787 , GRCh38 chr6: 1,744,004-2,006,554	GMDS
nsv4455720	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,910,715-2,150,669 , GRCh38.p12 chr6: 1,910,481-2,150,435	GMDS
nsv6636663	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,916,017-2,150,008 , GRCh38.p12 chr6: 1,915,783-2,149,774	GMDS
nsv4674961	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr6: 1,970,407-2,093,302 , GRCh38.p12 chr6: 1,970,173-2,093,068	GMDS
nsv3886705	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,875,823-1,964,471 , GRCh38.p12 chr6: 1,875,589-1,964,237	GMDS
nsv4456285	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 2,113,808-2,188,830 , GRCh38.p12 chr6: 2,113,574-2,188,596	GMDS
nsv6290852	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,705,438-1,767,134 , GRCh38.p12 chr6: 1,705,204-1,766,900	GMDS
nsv4675879	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 1,949,490-1,999,263 , GRCh38.p12 chr6: 1,949,256-1,999,029	GMDS
nsv5564350	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 1,611,031-1,611,082 , GRCh37 chr6: 1,611,266-1,611,317	FOXC1

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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 8942

Page of 448

Number of Variants: 20

Page of 448

Supplemental Content

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