spata2l[All Fields] AND 1[has_clinical] - 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
nsv3902265	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 89,762,136-89,764,596 , GRCh38.p12 chr16: 89,695,728-89,698,188	SPATA2L, CDK10
nsv3908665	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 89,762,056-89,790,048 , GRCh38.p12 chr16: 89,695,648-89,723,640	SPATA2L, VPS9D1-AS1, 3 more genes
nsv7095117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 89,712,474-89,866,066 , GRCh38.p12 chr16: 89,646,066-89,799,658	SPATA2L, FANCA, 7 more genes
nsv6112808	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 89,620,873-89,881,041 , GRCh38.p12 chr16: 89,554,465-89,814,633	SPATA2L, CHMP1A, 12 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	SPATA2L, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	SPATA2L, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	SPATA2L, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	SPATA2L, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	SPATA2L, FTLP14, 1868 more genes
nsv3921269	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345	SPATA2L, LOC105371237, 985 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	SPATA2L, ATMIN, 826 more genes
nsv3915506	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 51,490,596-88,682,563 , GRCh38 chr16: 52,899,183-90,088,654 , GRCh37 chr16: 52,933,095-90,155,062	SPATA2L, CFAP69P1, 716 more genes
nsv3891306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 57,051,473-89,797,669 , GRCh38.p12 chr16: 57,017,561-89,731,261	SPATA2L, LOC107984894, 613 more genes
nsv3913913	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 62,980,782-88,675,894 , GRCh38 chr16: 64,389,378-90,081,985 , GRCh37 chr16: 64,423,281-90,148,393	SPATA2L, ATP5F1AP3, 534 more genes
nsv3919817	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 63,904,799-88,675,894 , GRCh37 chr16: 65,347,298-90,148,393 , GRCh38 chr16: 65,313,395-90,081,985	SPATA2L, LOC105376772, 527 more genes
nsv3910304	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 64,102,887-88,690,904 , GRCh38 chr16: 65,511,483-90,096,995 , GRCh37 chr16: 65,545,386-90,163,403	SPATA2L, MC1R, 528 more genes
nsv3922616	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 70,514,631-90,081,985 , NCBI36 chr16: 69,106,035-88,675,894 , GRCh37 chr16: 70,548,534-90,148,393	SPATA2L, FOXF1, 367 more genes
nsv3922890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 70,783,301-90,163,403 , GRCh38 chr16: 70,749,398-90,096,995 , NCBI36 chr16: 69,340,802-88,690,904	SPATA2L, GCSH, 362 more genes
nsv3893537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 72,515,938-90,155,062 , GRCh38.p12 chr16: 72,482,039-90,088,654	SPATA2L, AFG3L1P, 316 more genes
nsv3897096	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 74,872,514-90,274,440 , GRCh38.p12 chr16: 74,838,616-90,208,032	SPATA2L, LOC105371394, 296 more genes

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Number of Variants: 20

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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

Search results

Items: 1 to 20 of 84

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Number of Variants: 20

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