b-Methoxy-9-BBN - 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
nsv4451832	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 132,896,215-132,928,892 , GRCh37 chr9: 135,771,602-135,804,279	TSC1
nsv3872348	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 132,896,229-132,928,878 , GRCh37 chr9: 135,771,616-135,804,265	TSC1
nsv4682244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,775,735-135,797,380 , GRCh38.p12 chr9: 132,900,348-132,921,993	TSC1
nsv3916188	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 107,524,001-107,543,399 , GRCh38 chr9: 105,721,899-105,741,297 , GRCh37 chr9: 108,484,180-108,503,578	TMEM38B
nsv4683975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,785,938-135,804,279 , GRCh38.p12 chr9: 132,910,551-132,928,892	TSC1
nsv5673820	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,782,098-135,796,843 , GRCh38.p12 chr9: 132,906,711-132,921,456	TSC1
nsv7097934	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,771,184-135,781,738 , GRCh38.p12 chr9: 132,895,797-132,906,351	TSC1
nsv6312849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,201,691-135,210,134 , GRCh38.p12 chr9: 132,326,304-132,334,747	SETX
nsv3878833	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,771,602-135,779,861 , GRCh38 chr9: 132,896,215-132,904,474	TSC1
nsv5381735	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 139,984,917-139,991,370 , GRCh38 chr9: 137,090,465-137,096,918	MAN1B1
nsv5564453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,777,972-135,782,777 , GRCh38.p12 chr9: 132,902,585-132,907,390	TSC1
nsv4681771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,771,602-135,776,244 , GRCh38.p12 chr9: 132,896,215-132,900,857	TSC1
nsv4728171	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 132,902,018-132,904,171 , GRCh37 chr9: 135,777,405-135,779,558	TSC1
nsv3873528	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 132,910,551-132,912,477 , GRCh37 chr9: 135,785,938-135,787,864	TSC1
nsv6313261	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,802,568-135,804,339 , GRCh38.p12 chr9: 132,927,181-132,928,952	TSC1
nsv4728593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,776,875-135,778,432 , GRCh38 chr9: 132,901,488-132,903,045	TSC1
nsv7098430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,771,622-135,773,017 , GRCh38.p12 chr9: 132,896,235-132,897,630	TSC1
nsv6312745	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 108,483,798-108,484,922 , GRCh38.p12 chr9: 105,721,517-105,722,641	TMEM38B
nsv4681344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 135,796,730-135,797,380 , GRCh38.p12 chr9: 132,921,343-132,921,993	TSC1
nsv6315259	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 105,640,632-105,641,104 , GRCh37 chr9: 108,402,913-108,403,385	FKTN

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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 112852

Page of 5643

Number of Variants: 20

Page of 5643

Supplemental Content

Find related data

Search details

Recent activity