"nstd102"[study] AND "normal"[Clinical Phenotype] AND "pregnancy"[Clin - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916643	copy number variation	2	nstd102	human	not provided, Benign	GRCh37 chr8: 137,688,230-137,857,327 , GRCh38 chr8: 136,675,987-136,845,084	LINC02055
nsv3917738	copy number variation	4	nstd102	human	not provided, Benign	GRCh38 chr10: 66,318,723-66,354,723 , GRCh37 chr10: 68,078,481-68,114,481	CTNNA3
nsv3873240	copy number variation	1	nstd102	human	not provided	GRCh38 chr18: 1,725,757-1,839,338 , GRCh37 chr18: 1,725,758-1,839,339	LOC105371959
nsv3872613	copy number variation	1	nstd102	human	not provided	GRCh38 chr6: 65,118,960-65,200,327 , GRCh37 chr6: 65,828,853-65,910,220	EYS
nsv3883540	copy number variation	2	nstd102	human	not provided	GRCh38 chr8: 16,090,726-16,168,455 , GRCh37 chr8: 15,948,235-16,025,964	MSR1
nsv3888290	copy number variation	1	nstd102	human	not provided	GRCh37 chr2: 51,345,474-51,411,126 , GRCh38 chr2: 51,118,336-51,183,988	NRXN1-DT
nsv3881052	copy number variation	1	nstd102	human	not provided	GRCh37 chr5: 97,048,466-97,111,523 , GRCh38 chr5: 97,712,762-97,775,819	LOC391813
nsv3887291	copy number variation	1	nstd102	human	not provided	GRCh38 chr16: 63,486,872-63,548,847 , GRCh37 chr16: 63,520,776-63,582,751	LOC105371308
nsv3875615	copy number variation	4	nstd102	human	not provided	GRCh37 chr5: 97,048,466-97,108,559 , GRCh38 chr5: 97,712,762-97,772,855	LOC391813
nsv3871349	copy number variation	1	nstd102	human	not provided	GRCh37 chr5: 97,047,653-97,099,320 , GRCh38 chr5: 97,711,949-97,763,616	LOC391813
nsv3886997	copy number variation	1	nstd102	human	not provided	GRCh38 chr4: 157,509,395-157,558,355 , GRCh37 chr4: 158,430,547-158,479,507	LOC107986238
nsv3884448	copy number variation	2	nstd102	human	not provided	GRCh38 chr3: 89,335,416-89,368,021 , GRCh37 chr3: 89,384,566-89,417,171	EPHA3
nsv3873930	copy number variation	3	nstd102	human	not provided	GRCh38 chr3: 165,323,328-165,355,218 , GRCh37 chr3: 165,041,116-165,073,006	LINC01322
nsv3879023	copy number variation	1	nstd102	human	not provided	GRCh38 chr17: 62,031,680-62,059,724 , GRCh37 chr17: 60,109,041-60,137,085	MED13
nsv3880755	copy number variation	2	nstd102	human	not provided	GRCh38 chr7: 17,386,271-17,413,855 , GRCh37 chr7: 17,425,895-17,453,479	LINC02888
nsv3887706	copy number variation	1	nstd102	human	not provided	GRCh38 chr6: 55,954,564-55,981,729 , GRCh37 chr6: 55,819,362-55,846,527	LOC107986539
nsv3876412	copy number variation	1	nstd102	human	not provided	GRCh37 chr16: 79,252,324-79,273,682 , GRCh38 chr16: 79,218,427-79,239,785	MAF
nsv3875762	copy number variation	4	nstd102	human	not provided	GRCh37 chr13: 69,247,022-69,267,981 , GRCh38 chr13: 68,672,890-68,693,849	RN7SL761P
nsv3874393	copy number variation	4	nstd102	human	not provided	GRCh38 chr7: 142,074,490-142,093,619 , GRCh37 chr7: 141,774,290-141,793,419	MGAM
nsv3884491	copy number variation	1	nstd102	human	not provided	GRCh37 chr7: 3,609,712-3,627,799 , GRCh38 chr7: 3,570,080-3,588,167	SDK1

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Organism

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Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 224

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Number of Variants: 20

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