STS - 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
nsv5381674	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 7,137,497-7,272,667 , GRCh38.p12 chrX: 7,219,456-7,354,626	STS
nsv6313234	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chrX: 7,137,717-7,268,302 , GRCh38.p12 chrX: 7,219,676-7,350,261	STS
nsv5381753	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 7,137,717-7,268,302 , GRCh38.p12 chrX: 7,219,676-7,350,261	STS
nsv3885671	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 7,143,912-7,185,127 , GRCh38.p12 chrX: 7,225,871-7,267,086	STS
nsv3891337	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 7,145,359-7,177,501 , GRCh38 chrX: 7,227,318-7,259,460 , NCBI36 chrX: 7,155,359-7,187,501	STS
nsv7098545	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 7,171,217-7,177,833 , GRCh38.p12 chrX: 7,253,176-7,259,792	STS
nsv3885862	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 7,269,569-7,706,446 , GRCh38.p12 chrX: 7,351,528-7,738,405	STS
nsv3870534	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 7,218,800-7,391,581 , GRCh38.p12 chrX: 7,300,759-7,473,540	STS
nsv3880064	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 7,113,308-7,255,259 , GRCh38.p12 chrX: 7,195,267-7,337,218	STS
nsv917640	copy number variation	1	nstd75	human		NCBI36 chrX: 7,206,060-7,704,191 , GRCh37.p13 chrX: 7,196,060-7,744,191 , GRCh38.p12 chrX: 7,278,019-7,776,150	STS
nsv917686	copy number variation	1	nstd75	human		NCBI36 chrX: 7,094,783-7,443,955 , GRCh37.p13 chrX: 7,084,783-7,433,955 , GRCh38.p12 chrX: 7,166,742-7,515,914	STS
nsv4728673	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,168,745-7,754,214 , GRCh38.p12 chrX: 7,250,704-7,786,173	STS
nsv3872687	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,153,846-7,469,635 , GRCh38.p12 chrX: 7,235,805-7,551,594	STS
nsv3900409	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 7,225,335-7,409,734 , GRCh37 chrX: 7,215,335-7,399,734 , GRCh38 chrX: 7,297,294-7,481,693	STS
nsv3897999	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 7,078,722-7,253,344 , GRCh38 chrX: 7,150,681-7,325,303 , GRCh37 chrX: 7,068,722-7,243,344	STS
nsv3873073	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,252,959-7,394,015 , GRCh38.p12 chrX: 7,334,918-7,475,974	STS
nsv4674520	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,252,959-7,391,892 , GRCh38.p12 chrX: 7,334,918-7,473,851	STS
nsv4728389	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,266,135-7,391,892 , GRCh38.p12 chrX: 7,348,094-7,473,851	STS
nsv4728185	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,266,135-7,366,211 , GRCh38.p12 chrX: 7,348,094-7,448,170	STS
nsv7098328	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 7,223,067-7,268,302 , GRCh38.p12 chrX: 7,305,026-7,350,261	STS

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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

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Items: 1 to 20 of 2302

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Number of Variants: 20

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