etv2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3919296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723	ETV2, UBA2, 241 more genes
nsv3916007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990	ETV2, MAG, 238 more genes
nsv4349605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090	ETV2, ATP4A, 129 more genes
nsv4350190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742	ETV2, SCN1B, 76 more genes
nsv4674329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397	ETV2, LOC105372379, 50 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ETV2, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	ETV2, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	ETV2, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	ETV2, BCKDHA, 1102 more genes
nsv6290300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324	ETV2, ZNF420, 574 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	ETV2, ZNF461, 735 more genes
nsv3906538	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 35,658,728-36,173,537 , GRCh38.p12 chr19: 35,167,825-35,682,635	ETV2, ATP4A, 33 more genes
nsv6310629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407	ETV2, KRTDAP, 78 more genes
nsv4457800	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984	ETV2, SBSN, 38 more genes
nsv7095478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407	ETV2, NFKBID, 141 more genes
nsv6291710	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 36,019,064-36,516,110 , GRCh38.p12 chr19: 35,528,162-36,025,208	ETV2, NFKBID, 38 more genes

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