thbs4[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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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
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	THBS4, 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	THBS4, 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	THBS4, 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	THBS4, 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	THBS4, 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	THBS4, LOC101929380, 318 more genes
nsv3921656	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 79,306,850-79,639,368 , GRCh37.p13 chr5: 79,271,094-79,603,612 , GRCh38.p12 chr5: 79,975,271-80,307,793	THBS4, LOC644936, 7 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	THBS4, RNU1-150P, 1757 more genes
nsv3914496	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,961,491-80,493,505 , NCBI36 chr5: 78,997,247-80,529,261 , GRCh38 chr5: 79,665,668-81,197,686	THBS4, ZFYVE16, 31 more genes
nsv6636970	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 79,153,778-79,683,392 , GRCh38.p12 chr5: 79,857,955-80,387,573	THBS4, RPL39P20, 14 more genes
nsv6313782	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 79,153,777-79,683,363 , GRCh38.p12 chr5: 79,857,954-80,387,544	THBS4, LINC01455, 14 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	THBS4, LOC105378993, 2492 more genes
nsv4455617	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 78,700,197-79,294,390 , GRCh38.p12 chr5: 79,404,374-79,998,567	THBS4, LOC102724557, 10 more genes

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