cntnap4[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
nsv3890892	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 76,514,714-76,635,963 , GRCh38.p12 chr16: 76,480,817-76,602,066	CNTNAP4
nsv3896550	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 76,540,062-76,552,331 , GRCh38.p12 chr16: 76,506,165-76,518,434	CNTNAP4
nsv3897097	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 76,535,342-76,544,758 , GRCh38.p12 chr16: 76,501,445-76,510,861	CNTNAP4
nsv3905022	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 76,442,956-76,451,047 , GRCh38.p12 chr16: 76,409,059-76,417,150	CNTNAP4
nsv3890945	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 76,540,062-76,544,758 , GRCh38.p12 chr16: 76,506,165-76,510,861	CNTNAP4
nsv4676063	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,324,005-76,656,042 , GRCh38.p12 chr16: 76,290,108-76,622,145	CNTNAP4
nsv6291671	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,457,786-76,610,695 , GRCh38.p12 chr16: 76,423,889-76,576,798	CNTNAP4
nsv6637216	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,575,950-76,638,633 , GRCh38.p12 chr16: 76,542,053-76,604,736	CNTNAP4
nsv4455776	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,348,941-76,374,538 , GRCh38.p12 chr16: 76,315,044-76,340,641	CNTNAP4
nsv3914395	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr16: 75,078,926-75,292,825 , GRCh37 chr16: 76,521,425-76,735,324 , GRCh38 chr16: 76,487,528-76,701,427	CNTNAP4, LINC02125
nsv3924711	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr16: 75,078,926-75,326,899 , GRCh37 chr16: 76,521,425-76,769,398 , GRCh38 chr16: 76,487,528-76,735,501	CNTNAP4, LINC02125
nsv3914183	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr16: 74,894,521-75,240,832 , GRCh37.p13 chr16: 76,337,020-76,683,331 , GRCh38.p12 chr16: 76,303,123-76,649,434	CNTNAP4, LINC02125
nsv3909962	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr16: 74,785,368-75,253,233 , GRCh37 chr16: 76,227,867-76,695,732 , GRCh38 chr16: 76,193,969-76,661,835	CNTNAP4, RN7SKP233, 2 more genes
nsv4455069	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,009,327-76,656,042 , GRCh38.p12 chr16: 75,975,429-76,622,145	CNTNAP4, RN7SKP233, 2 more genes
nsv3915883	copy number variation	1	nstd102	human	conflicting data from submitters	NCBI36 chr16: 74,624,569-75,139,600 , GRCh38 chr16: 76,033,170-76,548,202 , GRCh37 chr16: 76,067,068-76,582,099	CNTNAP4, RN7SKP233, 2 more genes
nsv3909427	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 76,000,179-76,371,082 , GRCh38.p12 chr16: 75,966,281-76,337,185	CNTNAP4, RN7SKP233, 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	CNTNAP4, 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	CNTNAP4, 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	CNTNAP4, TRG-GCC3-1, 137 more genes
nsv3909917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 75,575,400-79,188,037 , GRCh38 chr16: 75,541,502-79,154,140 , NCBI36 chr16: 74,132,901-77,745,538	CNTNAP4, LOC100131126, 40 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 69

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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