fam169a[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 11

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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
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	FAM169A, MEGF10, 2080 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	FAM169A, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	FAM169A, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	FAM169A, SPEF2, 2490 more genes
nsv3917856	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153	FAM169A, CSNK1A1P3, 413 more genes
nsv4675667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166	FAM169A, LOC101929380, 318 more genes
nsv4436202	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379	FAM169A, RNU1-150P, 1757 more genes
nsv3915627	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 74,028,621-74,115,824 , GRCh37.p13 chr5: 73,992,865-74,080,068 , GRCh38.p12 chr5: 74,697,040-74,784,243	FAM169A, RNU6-1330P, 4 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	FAM169A, LOC105378993, 2492 more genes
nsv4675088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 72,829,994-74,076,751 , GRCh38.p12 chr5: 73,534,169-74,780,926	FAM169A, NSA2, 17 more genes
nsv7097159	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr5: 73,980,960-75,008,762 , GRCh38.p12 chr5: 74,685,135-75,712,937	FAM169A, NSA2, 22 more genes

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