gdf5[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
nsv6310907	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 34,013,855-34,022,482 , GRCh38.p12 chr20: 35,426,058-35,434,684	GDF5, GDF5-AS1
nsv7096023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 34,021,707-34,025,983 , GRCh38.p12 chr20: 35,433,909-35,438,203	GDF5, GDF5-AS1
nsv997080	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr20: 34,021,145-34,042,568 , GRCh38.p12 chr20: 35,433,347-35,454,746	GDF5, CEP250, 2 more genes
nsv7095555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 34,021,707-34,067,990 , GRCh38.p12 chr20: 35,433,909-35,480,165	GDF5, CEP250-AS1, 3 more genes
nsv3912723	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019	GDF5, LOC107985448, 370 more genes
nsv3910049	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818	GDF5, NDUFB4P10, 291 more genes
nsv3913594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881	GDF5, AHCY, 93 more genes
nsv6311078	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288	GDF5, EDEM2, 93 more genes
nsv3910160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 33,336,941-33,796,173 , GRCh38 chr20: 35,285,724-35,744,837 , GRCh37 chr20: 33,873,527-34,332,759	GDF5, CPNE1, 19 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	GDF5, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	GDF5, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	GDF5, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	GDF5, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	GDF5, MIR3646, 1310 more genes
nsv3910142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013	GDF5, DYNLRB1, 555 more genes
nsv3918053	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426	GDF5, MYH7B, 300 more genes
nsv4457806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549	GDF5, EFCAB8, 162 more genes
nsv3920503	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528	GDF5, UQCC1, 111 more genes
nsv3913986	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 33,103,319-33,489,663 , GRCh37 chr20: 33,639,658-34,026,249 , GRCh38 chr20: 35,051,855-35,438,457	GDF5, EIF6, 12 more genes
nsv6637546	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323	GDF5, AHCY, 195 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 22

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Number of Variants: 20

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Search details

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