fam20a[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
nsv3881537	copy number variation	1	nstd102	human	not provided	GRCh38 chr17: 68,569,922-68,585,365 , GRCh37 chr17: 66,566,063-66,581,506	FAM20A
nsv7095362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 66,508,520-66,548,013 , GRCh38.p12 chr17: 68,512,379-68,551,872	FAM20A, PRKAR1A
nsv5672892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 66,508,520-66,533,875 , GRCh38.p12 chr17: 68,512,379-68,537,734	FAM20A, PRKAR1A
nsv3875057	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 66,508,520-66,526,600 , GRCh38 chr17: 68,512,379-68,530,459	FAM20A, PRKAR1A
nsv3883163	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 68,515,394-68,530,455 , GRCh37 chr17: 66,511,535-66,526,596	FAM20A, PRKAR1A
nsv3872661	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 68,515,384-68,529,001 , GRCh37 chr17: 66,511,525-66,525,142	FAM20A, PRKAR1A
nsv4682209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 66,518,887-66,526,600 , GRCh38.p12 chr17: 68,522,746-68,530,459	FAM20A, PRKAR1A
nsv6314992	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 68,534,265-68,541,795 , GRCh37 chr17: 66,530,406-66,537,936	FAM20A, PRKAR1A
esv3648840	copy number variation	1	estd216	human	not provided	GRCh37 chr17: 66,566,063-66,581,506 , GRCh38.p12 chr17: 68,569,922-68,585,365	FAM20A,
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	FAM20A, PRPSAP1, 1350 more genes
nsv3910890	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 68,420,514-71,351,235 , NCBI36 chr17: 63,928,250-66,858,971 , GRCh37 chr17: 66,416,655-69,347,376	FAM20A, KCNJ16, 34 more genes
nsv3921398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,829,982-68,081,995 , GRCh38 chr17: 67,833,866-70,085,854 , NCBI36 chr17: 63,260,444-65,593,590	FAM20A, LRRC37A16P, 41 more genes
nsv3920127	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 67,584,224-68,639,875 , NCBI36 chr17: 63,010,802-64,147,611 , GRCh37 chr17: 65,580,340-66,636,016	FAM20A, LOC101928045, 25 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	FAM20A, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	FAM20A, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	FAM20A, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	FAM20A, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	FAM20A, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	FAM20A, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	FAM20A, RNU6-131P, 1075 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 27

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Number of Variants: 20

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Supplemental Content

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