"nstd102"[study] AND "gestational"[Clinical Phenotype] AND "diabetes"[ - 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
nsv3879338	copy number variation	1	nstd102	human	not provided	GRCh38 chr8: 136,667,562-136,845,084 , GRCh37 chr8: 137,679,805-137,857,327	LINC02055
nsv3877543	copy number variation	1	nstd102	human	not provided	GRCh38 chr4: 92,865,624-93,026,952 , GRCh37 chr4: 93,786,775-93,948,103	GRID2
nsv3882870	copy number variation	1	nstd102	human	not provided	GRCh37 chr7: 10,819,155-10,945,193 , GRCh38 chr7: 10,779,528-10,905,566	MGC4859
nsv3883201	copy number variation	1	nstd102	human	not provided	GRCh38 chr9: 12,046,842-12,163,583 , GRCh37 chr9: 12,046,842-12,163,583	LOC105375976
nsv3875020	copy number variation	2	nstd102	human	not provided	GRCh38 chr11: 120,686,634-120,759,743 , GRCh37 chr11: 120,557,343-120,630,452	GRIK4
nsv3875626	copy number variation	1	nstd102	human	not provided	GRCh37 chr8: 86,923,375-86,990,451 , GRCh38 chr8: 85,911,146-85,978,222	LOC107986954
nsv3877240	copy number variation	1	nstd102	human	not provided	GRCh38 chr11: 122,815,420-122,878,506 , GRCh37 chr11: 122,686,128-122,749,214	CRTAM
nsv3872413	copy number variation	1	nstd102	human	not provided	GRCh38 chr16: 72,689,714-72,751,404 , GRCh37 chr16: 72,723,613-72,785,303	KRT18P18
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
nsv3887341	copy number variation	1	nstd102	human	not provided	GRCh37 chr19: 20,663,314-20,707,568 , GRCh38 chr19: 20,480,509-20,524,763	LOC105372316
nsv3876295	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 99,525,126-99,566,782 , GRCh38 chr11: 99,654,395-99,696,051	CNTN5
nsv3889927	copy number variation	1	nstd102	human	not provided	GRCh37 chr10: 68,078,481-68,113,595 , GRCh38 chr10: 66,318,723-66,353,837	CTNNA3
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
nsv3887242	copy number variation	1	nstd102	human	not provided	GRCh37 chr9: 28,309,788-28,342,179 , GRCh38 chr9: 28,309,790-28,342,181	LINGO2
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
nsv3881305	copy number variation	1	nstd102	human	not provided	GRCh37 chr2: 223,563,574-223,588,671 , GRCh38 chr2: 222,698,855-222,723,952	MOGAT1
nsv3878442	copy number variation	3	nstd102	human	not provided	GRCh38 chr19: 40,850,846-40,873,243 , GRCh37 chr19: 41,356,751-41,379,148	CYP2A6
nsv3877010	copy number variation	3	nstd102	human	not provided	GRCh38 chr5: 9,902,291-9,924,485 , GRCh37 chr5: 9,902,403-9,924,597	LINC02112
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
nsv3887051	copy number variation	1	nstd102	human	not provided	GRCh37 chr1: 36,367,780-36,387,654 , GRCh38 chr1: 35,902,179-35,922,053	AGO1

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Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 156

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Number of Variants: 20

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