galns[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
nsv6137674	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,813,734-88,842,705 , GRCh37.p13 chr16: 88,880,142-88,909,113	GALNS
nsv4682858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,888,977-88,909,257 , GRCh38.p12 chr16: 88,822,569-88,842,849	GALNS
nsv6137685	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,836,515-88,845,608 , GRCh37 chr16: 88,902,923-88,912,016	GALNS
nsv6137661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,819,654-88,825,599 , GRCh37 chr16: 88,886,062-88,892,007	GALNS
nsv4683623	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,904,010-88,909,257 , GRCh38.p12 chr16: 88,837,602-88,842,849	GALNS
nsv6137696	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,828,700-88,832,498 , GRCh37 chr16: 88,895,108-88,898,906	GALNS
nsv4451877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,907,380-88,909,257 , GRCh38 chr16: 88,840,972-88,842,849	GALNS
nsv4681383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,893,090-88,893,266 , GRCh38.p12 chr16: 88,826,682-88,826,858	GALNS
nsv5672851	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 88,893,090-88,904,193 , GRCh38.p12 chr16: 88,826,682-88,837,785	GALNS
nsv5672934	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 88,884,395-88,884,552 , GRCh38.p12 chr16: 88,817,987-88,818,144	GALNS
nsv6137664	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 88,904,029-88,904,172 , GRCh38 chr16: 88,837,621-88,837,764	GALNS
nsv3917342	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 88,885,164-88,902,647 , NCBI36 chr16: 87,412,665-87,430,148 , GRCh38 chr16: 88,818,756-88,836,239	GALNS
nsv3894843	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 88,891,364-88,902,183 , GRCh38.p12 chr16: 88,824,956-88,835,775	GALNS
nsv7095056	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 88,908,285-88,908,399 , GRCh38.p12 chr16: 88,841,877-88,841,991	GALNS
nsv6137658	complex substitution	1	nstd102	human	Uncertain significance	GRCh38 chr16: 88,825,006-88,836,241 , GRCh37.p13 chr16: 88,891,414-88,902,649	GALNS
nsv6137690	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,810,557-88,842,705 , GRCh37.p13 chr16: 88,876,965-88,909,113	GALNS, APRT
nsv6289968	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,770,428-88,832,724 , GRCh37.p13 chr16: 88,836,836-88,899,132	GALNS, CDT1, 2 more genes
nsv6137699	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 88,813,734-88,856,758 , GRCh37.p13 chr16: 88,880,142-88,923,166	GALNS, LOC107983950, 1 more genes
nsv3879349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,880,827-88,923,305 , GRCh38 chr16: 88,814,419-88,856,897	GALNS, TRAPPC2L, 1 more genes
nsv7098789	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,870,240-88,878,307 , GRCh38.p12 chr16: 88,803,832-88,811,899	GALNS, CDT1, 1 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

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Items: 1 to 20 of 116

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Number of Variants: 20

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