zfand2a[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
nsv3903996	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 1,126,463-1,194,990 , GRCh38.p12 chr7: 1,086,827-1,155,354	C7orf50, ZFAND2A, 2 more genes
nsv6636783	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 1,142,498-1,376,883 , GRCh38.p12 chr7: 1,102,862-1,337,247	UNCX, LOC102723758, 3 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	RNU6-438P, LOC105375300, 2682 more genes
nsv3920006	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 45,130-5,920,006 , GRCh38 chr7: 45,130-5,880,375 , NCBI36 chr7: 140,213-5,886,532	RNU6-215P, NUDT1, 120 more genes
nsv4456136	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536	LOC442497, LFNG, 85 more genes
nsv3894332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 1,201,674-5,175,651 , GRCh38.p12 chr7: 1,162,038-5,136,020	FOXK1, LOC107986759, 70 more genes
nsv3898790	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-3,642,604 , GRCh38.p12 chr7: 43,360-3,602,972	RPL21P72, FOXL3, 83 more genes
nsv3911664	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 54,185-3,324,143 , GRCh37 chr7: 54,185-3,363,775 , NCBI36 chr7: 149,268-3,330,301	MIR6836, CARD11, 81 more genes
nsv3912605	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 54,165-3,258,775 , NCBI36 chr7: 149,248-3,264,933 , GRCh37 chr7: 54,165-3,298,407	LOC100129603, LOC105375127, 80 more genes
nsv3916297	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr7: 54,185-1,843,584 , NCBI36 chr7: 149,268-1,849,746 , GRCh37 chr7: 54,185-1,883,220	MAD1L1, MIR4655, 51 more genes
nsv4675871	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161	C7orf50, LOC105375123, 47 more genes
nsv4675301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652	LOC112267991, MICALL2, 42 more genes
nsv3914197	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-1,480,761 , GRCh38 chr7: 54,185-1,441,125 , NCBI36 chr7: 149,268-1,447,287	LOC112267991, LOC442497, 34 more genes
nsv7097362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 193,200-1,498,962 , GRCh38.p12 chr7: 193,200-1,459,326	ZFAND2A-DT, MICALL2, 28 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	RNU6-565P, LAMB1, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	RPL23AP51, FLJ40288, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	MNX1-AS2, VN1R31P, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	TRGV3, SNX10-AS1, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	RPL23AP52, IQCE, 638 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	MMD2, ICA1-AS1, 554 more genes

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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 56

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Number of Variants: 20

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