ankrd6[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
nsv4729064	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 90,335,204-90,465,240 , GRCh38.p12 chr6: 89,625,485-89,755,521	ANKRD6, MDN1-AS1, 2 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	ANKRD6, LOC107986534, 426 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	ANKRD6, SPACA1, 187 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	ANKRD6, RNU4-72P, 157 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	ANKRD6, ME1, 136 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	ANKRD6, LOC105377882, 117 more genes
nsv3918084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697	ANKRD6, LOC105377897, 91 more genes
nsv3912992	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512	ANKRD6, DNAJC19P6, 88 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	ANKRD6, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	ANKRD6, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	ANKRD6, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ANKRD6, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	ANKRD6, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	ANKRD6, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	ANKRD6, ME1, 178 more genes
nsv3881379	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 90,157,697-90,395,016 , GRCh38.p12 chr6: 89,447,978-89,685,297	ANKRD6, MDN1, 4 more genes
nsv3880710	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 90,162,180-90,382,150 , GRCh38.p12 chr6: 89,452,461-89,672,431	ANKRD6, MDN1, 4 more genes
nsv3889895	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 89,941,373-95,634,177 , GRCh38.p12 chr6: 89,231,654-94,924,459	ANKRD6, RN7SKP110, 46 more genes
nsv3889103	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 90,296,588-90,646,226 , GRCh38.p12 chr6: 89,586,869-89,936,507	ANKRD6, LOC644269, 9 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	ANKRD6, MTHFD2P2, 212 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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