scand3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3873601	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 28,569,949-28,601,934 , GRCh38.p12 chr6: 28,602,172-28,634,157	TRA-AGC3-1, SCAND3, 1 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	LOC105378061, MIR4640, 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	RNU6-411P, LOC107986611, 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	SOD1P1, HLA-DPB1, 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	ITPR3, HSD17B8, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	TRR-ACG1-2, TMEM217, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	PRELID1P2, RPL7AP7, 785 more genes
nsv6289880	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408	ABCF1, AIF1, 313 more genes
nsv3870570	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590	LOC105375002, SKIC2, 345 more genes
nsv3911053	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069	GPX5, TRI-AAT9-1, 232 more genes
nsv3915580	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 28,516,623-28,779,629 , GRCh37.p13 chr6: 28,408,644-28,671,650 , GRCh38.p12 chr6: 28,440,867-28,703,873	SCAND3, TRK-TTT13-1, 24 more genes

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scand3[All Fields] AND 1[has_clinical] (12)
dbVar
Homo sapiens G protein subunit alpha q (GNAQ), mRNA
Homo sapiens G protein subunit alpha q (GNAQ), mRNA
gi|1653961273|ref|NM_002072.5|

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