znf135l[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	UBA2, ZNF529, 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	MAG, RNU6-967P, 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	LINC01531, FXYD5, 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	ATP4A, RNY5P10, 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	SCN1B, ETV2, 76 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	ZNF321P, ZNF861P, 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	BABAM1, BEST2, 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	LENG8, SYDE1, 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	BCKDHA, ADGRE5, 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	ZNF420, LOC105372330, 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	ZNF461, LOC101927572, 735 more genes
nsv3914228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054	LOC105372355, SUGP2, 411 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	ZNF599, FAM187B2P, 130 more genes
nsv3919618	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846	LINC00906, TDRD12, 112 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	NFKBID, LRP3, 141 more genes
nsv6314074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 32,827,535-35,263,640 , GRCh38.p12 chr19: 32,336,629-34,772,735	LOC100130632, CEP89, 59 more genes

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