znf91[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3904715	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 23,569,879-23,627,896 , GRCh38.p12 chr19: 23,387,077-23,445,094	ZNF91, VN1R92P, 2 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	ZNF91, 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	ZNF91, 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	ZNF91, 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	ZNF91, 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	ZNF91, ZNF420, 574 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	ZNF91, LOC105372355, 411 more genes
nsv3922457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424	ZNF91, REX1BD, 416 more genes
nsv3921076	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233	ZNF91, MRPL34, 358 more genes
nsv3895942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 16,526,787-24,631,604 , GRCh38.p12 chr19: 16,415,976-24,448,802	ZNF91, BNIP3P37, 307 more genes
nsv3909053	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 22,635,439-24,505,637 , GRCh38.p12 chr19: 22,452,637-24,322,835	ZNF91, RN7SL860P, 63 more genes
nsv4676147	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 22,630,650-24,487,350 , GRCh38.p12 chr19: 22,447,848-24,304,548	ZNF91, ZNF726P1, 64 more genes
nsv3894920	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 22,867,705-23,645,194 , GRCh38.p12 chr19: 22,684,903-23,462,392	ZNF91, ZNF730, 28 more genes
nsv6637478	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 23,217,767-23,956,831 , GRCh38.p12 chr19: 23,034,965-23,774,029	ZNF91, ZNF681, 27 more genes
nsv4436023	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 19,120,059-23,932,567 , GRCh37 chr19: 19,230,868-24,115,369	ZNF91, NCAN, 195 more genes

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