"nstd102"[study] AND "paternal"[Origin] - 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
nsv3922487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 124,437,486-124,820,793 , GRCh38 chr6: 124,116,341-124,499,647 , NCBI36 chr6: 124,479,185-124,862,492	NKAIN2
nsv3892943	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,710,306-50,999,091 , GRCh37 chr2: 50,937,444-51,226,229 , NCBI36 chr2: 50,790,948-51,079,733	NRXN1
nsv3917821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 68,968,673-69,158,502 , GRCh38 chr7: 69,865,751-70,055,580 , GRCh37 chr7: 69,330,737-69,520,566	AUTS2
nsv3890859	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 50,827,235-50,953,482 , GRCh37 chr2: 51,054,373-51,180,620 , NCBI36 chr2: 50,907,877-51,034,124	NRXN1
nsv7098962	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 31,762,447-31,872,385 , GRCh37.p13 chrX: 31,780,564-31,890,502	DMD
nsv6634326	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 129,376,140-129,458,794 , GRCh38.p12 chr6: 129,054,995-129,137,649	LAMA2
nsv4349618	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 83,664,877-83,740,076 , GRCh38.p12 chr7: 84,035,561-84,110,760	SEMA3A
nsv3912762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 34,150,132-34,182,300 , NCBI36 chr22: 32,480,132-32,512,300 , GRCh38 chr22: 33,754,145-33,786,313	LARGE1
nsv3887265	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 100,886,254-100,917,988 , GRCh38 chr12: 100,492,476-100,524,210	NR1H4
nsv7093261	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 78,375,608-78,407,230 , GRCh37.p13 chr16: 78,409,505-78,441,127	WWOX
nsv7098993	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 43,986,415-44,009,956 , GRCh37.p13 chr2: 44,213,554-44,237,095	LRPPRC
nsv6315171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 112,155,123-112,174,165 , GRCh38.p12 chr5: 112,819,426-112,838,468	APC
nsv6289911	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr14: 45,002,867-45,015,056 , GRCh37 chr14: 45,472,063-45,484,252	TOGARAM1
nsv5673749	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 70,232,101-70,241,078 , GRCh38 chr5: 70,936,274-70,945,251	SMN1
nsv7098778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 73,827,722-73,835,910 , GRCh38.p12 chr17: 75,831,641-75,839,829	UNC13D
nsv4728336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 48,271,306-48,278,757 , GRCh38.p12 chr17: 50,193,945-50,201,396	COL1A1
nsv7099022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 78,456,988-78,463,640 , GRCh38 chr16: 78,423,091-78,429,743	WWOX
nsv7098801	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 68,413,707-68,420,256 , GRCh37 chr10: 70,173,464-70,180,013	DNA2
nsv3883550	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 227,717,535-227,722,344 , GRCh37 chr2: 228,582,251-228,587,060	SLC19A3
nsv6635991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 121,434,542-121,438,222 , GRCh38 chr10: 119,675,030-119,678,710	BAG3

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dbVar

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 1291

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Number of Variants: 20

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