dspp[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
nsv6634526	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr4: 87,615,921-87,615,974 , GRCh37 chr4: 88,537,073-88,537,126	DSPP
nsv6634714	insertion	2	nstd102	human	Pathogenic	GRCh37 chr4: 88,537,232-88,537,232 , GRCh38 chr4: 87,616,080-87,616,080	DSPP
nsv6137653	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 88,537,151-88,537,240 , GRCh38 chr4: 87,615,999-87,616,088	DSPP
nsv6137790	copy number variation	3	nstd102	human	Pathogenic, Benign	GRCh37 chr4: 88,537,152-88,537,232 , GRCh38 chr4: 87,616,000-87,616,080	DSPP
nsv6137791	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr4: 87,616,026-87,616,097 , GRCh37 chr4: 88,537,178-88,537,249	DSPP
nsv6291324	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 88,483,563-88,544,373 , GRCh38.p12 chr4: 87,562,411-87,623,221	DSPP
nsv4435959	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr4: 87,616,116-87,616,268 , GRCh37 chr4: 88,537,268-88,537,420	DSPP
nsv4436505	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr4: 87,616,124-87,616,253 , GRCh37 chr4: 88,537,276-88,537,405	DSPP
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	DSPP, EREG, 530 more genes
nsv3923733	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621	DSPP, PDLIM5, 215 more genes
nsv7148241	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930	DSPP, LOC105377327, 214 more genes
nsv3888958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500	DSPP, LOC391674, 156 more genes
nsv6313484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074	DSPP, LOC105377329, 166 more genes
nsv3912429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447	DSPP, RNU6-469P, 152 more genes
nsv6291249	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,467,886-93,362,064 , GRCh38.p12 chr4: 79,546,732-92,440,913	DSPP, HNRNPA3P13, 155 more genes
nsv3916835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,496,902-93,333,600 , GRCh38 chr4: 79,575,748-92,412,449 , NCBI36 chr4: 80,715,926-93,552,623	DSPP, SLC10A6, 155 more genes
nsv4436731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 80,482,400-92,572,499 , GRCh38.p12 chr4: 79,561,246-91,651,348	DSPP, HERC5, 150 more genes
nsv6313848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270	DSPP, RPL6P13, 136 more genes
nsv3915919	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 85,469,728-94,794,648 , GRCh37.p13 chr4: 85,250,704-94,575,625 , GRCh38.p12 chr4: 84,329,551-93,654,474	DSPP, RNU6-907P, 89 more genes
nsv3910328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 86,370,518-94,894,345 , GRCh38 chr4: 85,449,365-93,973,194 , NCBI36 chr4: 86,589,542-95,113,368	DSPP, LOC112268468, 81 more genes

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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 37

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Number of Variants: 20

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Supplemental Content

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Search details

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