rcn3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 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	SNAP47, STK40, 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	RNU1-153P, MIR3917, 4887 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	RCN3, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	RCN3, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	RCN3, LENG8, 2408 more genes
nsv3901163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 24,707,696-41,886,350 , GRCh38 chr1: 24,381,206-41,401,517 , NCBI36 chr1: 24,580,283-41,658,937	TMEM222, ZBTB8OS, 453 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	RCN3, KCNA7, 697 more genes
nsv3911950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965	RCN3, LOC107987270, 694 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	RCN3, MIR4324, 485 more genes
nsv4729755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886	RCN3, SIGLEC5, 574 more genes
nsv6313906	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185	RCN3, AP2A1, 212 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	LINC01776, IGSF21-AS1, 1853 more genes
nsv4685764	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460	RCN3, SNAR-G1, 453 more genes
nsv4457465	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 49,600,909-51,366,070 , GRCh38.p12 chr19: 49,097,652-50,862,814	RCN3, MED25, 117 more genes
nsv6310544	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758	RCN3, CGB5, 76 more genes
nsv4684226	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,394,811-25,148,686 , GRCh38.p12 chr1: 24,068,321-24,822,195	GRHL3, CLIC4, 16 more genes
nsv6636637	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 24,363,507-24,875,537 , GRCh38.p12 chr1: 24,037,017-24,549,046	LOC105376864, GRHL3, 13 more genes

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rcn3[All Fields] AND 1[has_clinical] (19)
dbVar
Hypleurochilus multifilis voucher RIE_4176 recombination activating protein 1 (R...
Hypleurochilus multifilis voucher RIE_4176 recombination activating protein 1 (RAG1) gene, RAG1-A allele, partial cds
gi|2553036176|gb|OQ753667.1|

Nucleotide
recombination activating protein 1, partial [Blennius multifilis]
recombination activating protein 1, partial [Blennius multifilis]
gi|2553036193|gb|WKW49154.1|

Protein
cardiac muscle myosin heavy chain 6 alpha, partial [Blennius multifilis]
cardiac muscle myosin heavy chain 6 alpha, partial [Blennius multifilis]
gi|2553036295|gb|WKW49205.1|

Protein
LOC17884861 [Capsella rubella]
LOC17884861 [Capsella rubella]
Gene ID:17884861

Gene

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