3-Hydroxyethoxy-1-hydroxyethylbenzen diether - 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
nsv3881933	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 70,992,485-71,180,270 , GRCh37 chr3: 71,041,636-71,229,421	FOXP1
nsv3878398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 51,062,402-51,232,768 , GRCh38.p12 chr3: 51,024,971-51,195,337	DOCK3
nsv4674612	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 71,081,905-71,227,572 , GRCh38.p12 chr3: 71,032,754-71,178,421	FOXP1
nsv7096699	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr3: 154,801,957-154,898,248 , GRCh38.p12 chr3: 155,084,168-155,180,459	MME
nsv3873046	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 176,854,043-176,941,772 , GRCh38.p12 chr3: 177,136,255-177,223,984	TBL1XR1
nsv6311690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 38,591,802-38,674,808 , GRCh38.p12 chr3: 38,550,311-38,633,317	SCN5A
nsv7097216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 81,691,922-81,754,774 , GRCh38.p12 chr3: 81,642,771-81,705,623	GBE1
nsv6313809	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 71,251,088-71,312,384 , GRCh38.p12 chr3: 71,201,937-71,263,233	FOXP1
nsv7096453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,769,927-182,817,228 , GRCh38.p12 chr3: 183,052,139-183,099,440	MCCC1
nsv7097199	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 4,669,427-4,715,091 , GRCh38.p12 chr3: 4,627,743-4,673,407	ITPR1
nsv4769297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,902,731-182,945,128 , GRCh38.p12 chr3: 183,184,943-183,227,340	MCF2L2
nsv3871884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 71,008,556-71,049,017 , GRCh38.p12 chr3: 70,959,405-70,999,866	FOXP1
nsv6311880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 52,172,193-52,212,093 , GRCh38.p12 chr3: 52,138,177-52,178,077	POC1A
nsv7148225	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 25,699,606-25,738,988 , GRCh37.p13 chr3: 25,741,097-25,780,479	NGLY1
nsv7096949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 171,376,983-171,410,252 , GRCh38.p12 chr3: 171,659,193-171,692,462	PLD1
nsv7096936	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 136,002,659-136,035,926 , GRCh38.p12 chr3: 136,283,817-136,317,084	PCCB
nsv6311984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 38,616,768-38,649,725 , GRCh38.p12 chr3: 38,575,277-38,608,234	SCN5A
nsv5673718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 121,973,037-122,004,038 , GRCh38.p12 chr3: 122,254,190-122,285,191	CASR
nsv3881909	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 69,985,770-70,014,477 , GRCh38 chr3: 69,936,619-69,965,326	MITF
nsv6311777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 135,974,688-136,003,251 , GRCh38.p12 chr3: 136,255,846-136,284,409	PCCB

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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 101909

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Number of Variants: 20

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Supplemental Content

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