fig4[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
nsv6312131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,048,292-110,098,283 , GRCh38.p12 chr6: 109,727,089-109,777,080	FIG4
nsv6312223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,048,292-110,053,276 , GRCh38.p12 chr6: 109,727,089-109,732,073	FIG4
nsv3879063	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,062,627-110,064,995 , GRCh38 chr6: 109,741,424-109,743,792	FIG4
nsv3875486	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr6: 110,113,784-110,113,868 , GRCh38.p12 chr6: 109,792,581-109,792,665	FIG4
nsv7097035	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 110,081,433-110,088,118 , GRCh38.p12 chr6: 109,760,230-109,766,915	FIG4
nsv3882676	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 110,050,042-110,117,170 , GRCh38.p12 chr6: 109,728,839-109,795,967	FIG4
nsv4456015	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,141,405-110,220,627 , GRCh38.p12 chr6: 109,820,202-109,899,424	FIG4
nsv7097036	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,106,153-110,113,887 , GRCh38.p12 chr6: 109,784,950-109,792,684	FIG4
nsv4681413	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,146,281-110,146,478 , GRCh38.p12 chr6: 109,825,078-109,825,275	FIG4
nsv7097307	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,106,153-110,146,468 , GRCh38.p12 chr6: 109,784,950-109,825,265	FIG4
nsv7097175	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,117,948-110,118,074 , GRCh38.p12 chr6: 109,796,745-109,796,871	FIG4
nsv6312222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,012,639-110,064,995 , GRCh38.p12 chr6: 109,691,436-109,743,792	FIG4, AK9
nsv3882702	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 110,012,619-110,012,724 , GRCh38 chr6: 109,691,416-109,691,521	FIG4, AK9
nsv3916930	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 110,039,965-110,177,267 , GRCh37 chr6: 109,933,272-110,070,574 , GRCh38 chr6: 109,612,069-109,749,371	FIG4, AK9
nsv4675543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 109,920,344-110,080,533 , GRCh38.p12 chr6: 109,599,141-109,759,330	FIG4, AK9
nsv6290760	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 109,920,345-110,080,533 , GRCh38.p12 chr6: 109,599,142-109,759,330	FIG4, AK9
nsv6636354	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 109,925,791-110,080,533 , GRCh38.p12 chr6: 109,604,588-109,759,330	FIG4, AK9
nsv7097174	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,012,639-110,098,283 , GRCh38.p12 chr6: 109,691,436-109,777,080	FIG4, AK9
nsv3912258	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 110,208,809-110,630,205 , GRCh38 chr6: 109,780,913-110,202,309 , GRCh37 chr6: 110,102,116-110,523,512	FIG4, WASF1, 3 more genes
nsv3885190	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 110,080,484-110,472,732 , GRCh38.p12 chr6: 109,759,281-110,151,529	FIG4, GPR6, 2 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

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Items: 1 to 20 of 51

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Number of Variants: 20

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