meox1[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
nsv7095169	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,738,414-41,738,902 , GRCh38.p12 chr17: 43,661,046-43,661,534	MEOX1
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	MEOX1, PRPSAP1, 1350 more genes
nsv3919609	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 41,648,246-42,839,745 , GRCh38 chr17: 43,570,878-44,762,377 , NCBI36 chr17: 39,003,772-40,195,271	MEOX1, SMCO4P1, 59 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	MEOX1, 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	MEOX1, 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	MEOX1, 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	MEOX1, 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	MEOX1, LOC105371922, 1855 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	MEOX1, RNU6-131P, 1075 more genes
nsv3911563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214	MEOX1, PLEKHH3, 958 more genes
nsv3911344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579	MEOX1, IFI35, 345 more genes
nsv3920812	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr17: 43,322,528-43,849,385 , NCBI36 chr17: 38,755,418-39,282,279 , GRCh37 chr17: 41,399,892-41,926,753	MEOX1, LINC02594, 22 more genes
nsv3908708	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 41,464,491-41,835,873 , GRCh38.p12 chr17: 43,387,123-43,758,505	MEOX1, RNU6-971P, 15 more genes
nsv3907487	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 41,540,257-42,044,249 , GRCh38.p12 chr17: 43,462,889-43,966,881	MEOX1, PPY, 22 more genes
nsv3921716	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 38,456,488-39,330,777 , GRCh38 chr17: 43,050,945-43,897,883 , GRCh37 chr17: 41,202,962-41,975,251	MEOX1, LINC02594, 33 more genes
nsv6314057	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 41,202,796-41,974,964 , GRCh38.p12 chr17: 43,050,779-43,897,596	MEOX1, TMEM106A, 33 more genes
nsv3923117	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 43,080,123-43,897,875 , NCBI36 chr17: 38,485,666-39,330,769 , GRCh37 chr17: 41,232,140-41,975,243	MEOX1, RNU6-470P, 33 more genes
nsv3922353	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 43,088,882-43,865,172 , GRCh37 chr17: 41,240,899-41,942,540 , NCBI36 chr17: 38,494,425-39,298,066	MEOX1, NBR1, 31 more genes
nsv4674980	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 41,399,892-42,125,780 , GRCh38.p12 chr17: 43,322,528-44,048,412	MEOX1, RPL29P31, 34 more genes
nsv4729870	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 41,221,565-41,775,043 , GRCh38.p12 chr17: 43,069,548-43,697,675	MEOX1, LOC105371785, 24 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 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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