zfp1[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
nsv3909696	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 75,040,327-75,237,490 , GRCh38.p12 chr16: 75,006,429-75,203,592	ZFP1, RPS4Y1P1, 3 more genes
nsv6637472	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 75,164,013-75,256,868 , GRCh38.p12 chr16: 75,130,115-75,222,970 , GRCh38.p12 chr16\|NW_018654723.1: 1-53,168	ZFP1, RPS4Y1P1, 2 more genes
nsv3921095	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 69,005,977-83,499,227 , GRCh38 chr16: 70,414,573-84,908,120 , GRCh37 chr16: 70,448,476-84,941,726	ZFP1, NECAB2, 219 more genes
nsv3918168	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 71,640,867-81,167,432 , GRCh38 chr16: 73,049,467-82,576,326 , GRCh37 chr16: 73,083,366-82,609,931	ZFP1, BCAR1, 125 more genes
nsv3917504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,951,979-76,757,245 , NCBI36 chr16: 68,509,480-75,314,746 , GRCh38 chr16: 69,918,076-76,723,348	ZFP1, TRG-GCC3-1, 137 more genes
nsv3916803	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298	ZFP1, AP1G1, 138 more genes
nsv6309925	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 74,748,068-75,513,746 , GRCh38.p12 chr16: 74,714,170-75,479,848	ZFP1, CTRB1, 14 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	ZFP1, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	ZFP1, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	ZFP1, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	ZFP1, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	ZFP1, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	ZFP1, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	ZFP1, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	ZFP1, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	ZFP1, LOC107984894, 613 more genes
nsv3913913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393	ZFP1, ATP5F1AP3, 534 more genes
nsv3919817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985	ZFP1, LOC105376772, 527 more genes
nsv3910304	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403	ZFP1, MC1R, 528 more genes
nsv3920399	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 61,517,334-83,176,902 , GRCh37 chr16: 62,959,833-84,619,401 , GRCh38 chr16: 62,925,929-84,585,795	ZFP1, LOC654780, 385 more genes

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Number of Variants: 20

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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

Search results

Items: 1 to 20 of 57

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Number of Variants: 20

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