fxyd3[All Fields] AND 1[has_clinical] - 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
nsv3897154	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,612,084-35,622,065 , GRCh38.p12 chr19: 35,121,180-35,131,161	FXYD3, MIR6887, 1 more genes
nsv3896985	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,612,084-35,617,093 , GRCh38.p12 chr19: 35,121,180-35,126,189	FXYD3, LGI4, 1 more genes
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	FXYD3, 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	FXYD3, MAG, 238 more genes
nsv3918197	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 31,367,353-35,417,098 , NCBI36 chr19: 36,550,099-40,599,840 , GRCh37 chr19: 31,858,259-35,908,000	FXYD3, LINC01531, 110 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, 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	FXYD3, ZNF461, 735 more genes
nsv3900139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 30,735,448-36,120,396 , GRCh38.p12 chr19: 30,244,541-35,629,494	FXYD3, ZNF599, 130 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	FXYD3, 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	FXYD3, 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	FXYD3, NFKBID, 141 more genes
nsv1398275	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,516,999-35,990,896 , GRCh38.p12 chr19: 35,026,095-35,499,994	FXYD3, LOC105372380, 30 more genes
nsv4457758	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 35,548,527-35,772,471 , GRCh38.p12 chr19: 35,057,623-35,281,568	FXYD3, LOC105372379, 15 more genes

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Items: 20

Number of Variants: 20

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