abhd6[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960	ABHD6, LOC105377171, 323 more genes
nsv3919181	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176	ABHD6, MAGI1-AS1, 135 more genes
nsv4452524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281	ABHD6, LOC105377114, 110 more genes
nsv3875047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 52,086,599-59,689,209 , GRCh38.p12 chr3: 52,052,583-59,703,483	ABHD6, SLMAP, 132 more genes
nsv3917204	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197	ABHD6, C3orf49, 93 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	ABHD6, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	ABHD6, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	ABHD6, RPL23AP49, 2875 more genes
nsv3886371	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 58,089,516-58,799,748 , GRCh38.p12 chr3: 58,103,789-58,814,022	ABHD6, ACOX2, 18 more genes
nsv7097210	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 57,130,421-58,520,833 , GRCh38.p12 chr3: 57,096,393-58,535,106	ABHD6, LOC107984079, 37 more genes
nsv3921125	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 57,897,017-58,395,655 , NCBI36 chr3: 57,872,057-58,370,695 , GRCh38 chr3: 57,911,290-58,409,928	ABHD6, HTD2, 11 more genes
nsv4728391	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 57,912,545-58,357,970 , GRCh38.p12 chr3: 57,926,818-58,372,243	ABHD6, SLMAP, 10 more genes

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