st3gal6[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	ST3GAL6, NECTIN3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	ST3GAL6, MTCO2P29, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	ST3GAL6, ATP6V1A, 297 more genes
nsv3910775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886	ST3GAL6, ZBTB11-AS1, 258 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	ST3GAL6, 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	ST3GAL6, 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	ST3GAL6, RPL23AP49, 2875 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	ST3GAL6, OR7E53P, 794 more genes
nsv4728581	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282	ST3GAL6, COL8A1, 107 more genes
nsv6314751	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914	ST3GAL6, AKR1B1P2, 231 more genes
nsv3911724	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749	ST3GAL6, COL8A1, 132 more genes
nsv4728584	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 98,416,960-98,618,961 , GRCh38.p12 chr3: 98,698,116-98,900,117	ST3GAL6, PDLIM1P4, 4 more genes
nsv4674762	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 97,606,054-98,499,715 , GRCh38.p12 chr3: 97,887,210-98,780,871	ST3GAL6, OR5H4P, 36 more genes

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