sycp3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3903461	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 102,104,989-102,151,344 , GRCh38.p12 chr12: 101,711,211-101,757,566	SYCP3, RNY1P16, 2 more genes
nsv3899505	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 102,104,989-102,130,176 , GRCh38.p12 chr12: 101,711,211-101,736,398	SYCP3, CHPT1, 1 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	SYCP3, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	SYCP3, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	SYCP3, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	SYCP3, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	SYCP3, OR5BT1P, 2441 more genes
nsv3924338	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015	SYCP3, NUP37, 295 more genes
nsv3900015	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 94,881,995-103,635,998 , GRCh38.p12 chr12: 94,488,219-103,242,220	SYCP3, CDK17, 140 more genes
nsv6313913	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 100,564,593-103,021,075 , GRCh38.p12 chr12: 100,170,815-102,627,297	SYCP3, DEPDC4, 46 more genes
nsv4675271	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 101,953,283-102,683,945 , GRCh38.p12 chr12: 101,559,505-102,290,167	SYCP3, DRAM1, 23 more genes
nsv3907610	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 100,580,198-105,804,075 , GRCh38.p12 chr12: 100,186,420-105,410,297	SYCP3, ASCL1, 87 more genes
nsv4456033	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 101,447,925-102,593,349 , GRCh38.p12 chr12: 101,054,147-102,199,571	SYCP3, RPS27P23, 33 more genes
nsv4456023	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 102,116,591-102,607,083 , GRCh38.p12 chr12: 101,722,813-102,213,305	SYCP3, RNU6-172P, 16 more genes

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sycp3[All Fields] AND 1[has_clinical] (15)
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