arhgap6[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
nsv3892249	copy number variation	1	nstd102	human	Benign	NCBI36 chrX: 11,551,293-11,591,852 , GRCh38 chrX: 11,623,252-11,663,811 , GRCh37 chrX: 11,641,372-11,681,931	ARHGAP6
nsv3876199	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 11,314,055-11,318,781 , GRCh38 chrX: 11,295,935-11,300,661	ARHGAP6, AMELX
nsv4451978	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 11,091,134-11,291,611 , GRCh38.p12 chrX: 11,073,014-11,273,491	ARHGAP6, HCCS
nsv3876617	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chrX: 11,091,133-11,291,610 , GRCh38.p12 chrX: 11,073,013-11,273,490	ARHGAP6, HCCS
nsv3906961	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 11,038,216-11,190,005 , NCBI36 chrX: 10,966,257-11,118,046 , GRCh37 chrX: 11,056,336-11,208,125	ARHGAP6, HCCS
nsv3899093	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 11,023,814-11,168,204 , GRCh38 chrX: 11,095,773-11,240,163 , GRCh37 chrX: 11,113,893-11,258,283	ARHGAP6, HCCS
nsv3886386	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 11,285,049-11,381,288 , GRCh38 chrX: 11,266,933-11,363,172	ARHGAP6, GOT2P7, 2 more genes
nsv3916348	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 11,600,773-12,249,902 , GRCh38.p12 chrX: 11,582,653-12,231,783	ARHGAP6, FRMPD4, 3 more genes
nsv3910675	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 11,633,731-11,797,224 , GRCh38.p12 chrX: 11,615,611-11,779,105	ARHGAP6, MSL3, 2 more genes
nsv3881671	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 10,810,471-11,339,263 , GRCh38.p12 chrX: 10,792,352-11,321,143	ARHGAP6, AMELX, 3 more genes
nsv3871693	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 10,989,343-11,572,991 , GRCh38.p12 chrX: 10,971,223-11,554,871	ARHGAP6, HCCS, 3 more genes
nsv3882331	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 11,644,490-12,054,572 , GRCh38.p12 chrX: 11,626,370-12,036,453	ARHGAP6, LIMK2P1, 3 more genes
nsv3888865	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 11,532,401-11,935,042 , GRCh38.p12 chrX: 11,514,281-11,916,923	ARHGAP6, LIMK2P1, 3 more genes
nsv3888426	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 11,544,117-11,935,042 , GRCh38.p12 chrX: 11,525,997-11,916,923	ARHGAP6, LIMK2P1, 3 more genes
nsv4768361	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 10,578,932-11,326,337 , GRCh38.p12 chrX: 10,610,892-11,308,217	ARHGAP6, AMELX, 2 more genes
nsv3908645	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 10,472,724-11,073,546 , GRCh37 chrX: 10,512,724-11,163,625 , GRCh38 chrX: 10,544,684-11,145,505	ARHGAP6, MID1, 2 more genes
nsv3895994	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 11,586,685-12,102,545 , GRCh37 chrX: 11,676,764-12,192,624 , GRCh38 chrX: 11,658,644-12,174,505	ARHGAP6, MSL3, 3 more genes
nsv6290445	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 11,664,613-12,174,602 , GRCh37.p13 chrX: 11,682,733-12,192,721	ARHGAP6, LIMK2P1, 3 more genes
nsv3916359	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 11,096,826-11,546,659 , GRCh37.p13 chrX: 11,186,905-11,636,738 , GRCh38.p12 chrX: 11,168,785-11,618,618	ARHGAP6, MIR548AX, 2 more genes
nsv6636127	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 11,035,791-11,457,856 , GRCh38.p12 chrX: 11,017,671-11,439,736	ARHGAP6, AMELX, 3 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 195

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Number of Variants: 20

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