aknad1[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
nsv3885104	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 109,367,944-109,371,874 , GRCh38.p12 chr1: 108,825,322-108,829,252	AKNAD1, LOC105378891
nsv6636972	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 109,345,620-109,404,928 , GRCh38.p12 chr1: 108,802,998-108,862,306	AKNAD1, STXBP3, 2 more genes
nsv6313675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309	AKNAD1, LINC01307, 320 more genes
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	AKNAD1, AMYP1, 320 more genes
nsv3893941	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 97,648,746-111,014,655 , GRCh37 chr1: 97,876,158-111,213,132 , GRCh38 chr1: 97,410,602-110,670,510	AKNAD1, RPSAP19, 196 more genes
nsv3909776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 97,737,905-109,435,760 , GRCh38 chr1: 97,272,349-108,893,138 , NCBI36 chr1: 97,510,493-109,237,283	AKNAD1, SNX7, 133 more genes
nsv3901500	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 101,856,241-112,047,173 , GRCh38 chr1: 101,618,097-111,703,028 , GRCh37 chr1: 102,083,653-112,245,650	AKNAD1, CHIAP1, 171 more genes
nsv3920130	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 103,429,843-112,252,782 , GRCh37.p13 chr1: 103,657,255-112,451,259 , GRCh38.p12 chr1: 103,191,699-111,908,637	AKNAD1, LOC105378898, 166 more genes
nsv3901806	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 105,812,437-112,534,771 , GRCh38 chr1: 105,468,292-112,190,626 , GRCh37 chr1: 106,010,914-112,733,248	AKNAD1, LOC126987, 151 more genes
nsv3909407	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 106,617,209-110,686,912 , GRCh38 chr1: 106,074,587-110,144,290 , NCBI36 chr1: 106,418,732-110,488,435	AKNAD1, PSMA5, 81 more genes
nsv7095739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 108,679,275-111,674,176 , GRCh38.p12 chr1: 108,136,653-111,131,554	AKNAD1, RPL7L1P21, 90 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	AKNAD1, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	AKNAD1, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	AKNAD1, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	AKNAD1, LINC02607, 513 more genes
nsv3884558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 94,054,724-111,671,707 , GRCh38.p12 chr1: 93,589,167-111,129,085	AKNAD1, SLC25A24, 265 more genes
nsv3890331	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655	AKNAD1, OR11I1P, 324 more genes
nsv3875681	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr1: 103,175,204-111,410,059 , GRCh37.p13 chr1: 103,640,760-111,952,681	AKNAD1, ALX3, 146 more genes
nsv4436700	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 107,779,092-111,199,205 , GRCh38.p12 chr1: 107,236,470-110,656,583	AKNAD1, ALX3, 89 more genes
nsv4453642	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 108,926,313-111,266,497 , GRCh38.p12 chr1: 108,383,691-110,723,875	AKNAD1, PSMA5, 79 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 30

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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