ngdn[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
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	NGDN, HNRNPC, 616 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	NGDN, MIR208B, 600 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	NGDN, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	NGDN, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	NGDN, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	NGDN, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	NGDN, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	NGDN, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	NGDN, MIR656, 1918 more genes
nsv3913204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995	NGDN, SMARCE1P3, 635 more genes
nsv6315513	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000	NGDN, CDH24, 623 more genes
nsv4675943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827	NGDN, TRAJ36, 590 more genes
nsv3918965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625	NGDN, TRAJ13, 589 more genes
nsv3912710	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,000,611-38,984,415 , NCBI36 chr14: 19,538,610-38,523,370 , GRCh37 chr14: 20,468,770-39,453,619	NGDN, UBE2NP1, 553 more genes
nsv3898685	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-34,049,214 , GRCh38.p12 chr14: 19,652,445-33,580,008	NGDN, LOC105370419, 480 more genes
nsv4349901	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881	NGDN, TRAV4, 458 more genes
nsv3898291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-27,768,254 , GRCh38.p12 chr14: 19,652,445-27,299,048	NGDN, HOMEZ, 411 more genes
nsv3922265	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120	NGDN, ANG, 346 more genes
nsv4578270	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011	NGDN, BCL2L2, 215 more genes
nsv3895712	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 23,840,034-24,057,640 , GRCh38.p12 chr14: 23,370,825-23,588,431	NGDN, MYH6, 11 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 23

Page of 2

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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