nkx2-6[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
nsv3888378	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr8: 23,671,119-23,712,463 , GRCh37 chr8: 23,528,632-23,569,976	NKX2-6, NKX3-1, 2 more genes
nsv6636443	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 23,502,588-23,680,392 , GRCh38.p12 chr8: 23,645,075-23,822,879	NKX2-6, LOC101929258, 2 more genes
nsv6315449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940	NKX2-6, LOC101928016, 568 more genes
nsv3917350	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713	NKX2-6, LINC03022, 472 more genes
nsv7148253	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417	NKX2-6, ENTPD4, 447 more genes
nsv7148146	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253	NKX2-6, LOC101929028, 274 more genes
nsv3916527	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 15,137,722-32,366,274 , GRCh37.p13 chr8: 15,093,351-32,246,732 , GRCh38.p12 chr8: 15,235,842-32,389,216	NKX2-6, LOC105379343, 281 more genes
nsv3921296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 12,383,584-29,033,946 , NCBI36 chr8: 12,285,464-28,947,382 , GRCh37 chr8: 12,241,093-28,891,463	NKX2-6, XPO7, 264 more genes
nsv3923174	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324	NKX2-6, RPLP1P9, 259 more genes
nsv3896830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 13,091,530-24,483,615 , GRCh38.p12 chr8: 13,234,021-24,626,102	NKX2-6, LOC105379297, 161 more genes
nsv4455606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 22,442,548-27,369,334 , GRCh38.p12 chr8: 22,585,035-27,511,817	NKX2-6, PPP2R2A, 91 more genes
nsv4457159	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 21,662,847-24,199,218 , GRCh38.p12 chr8: 21,805,335-24,341,705	NKX2-6, SINHCAFP3, 66 more genes
nsv4456504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 23,501,519-24,907,990 , GRCh38.p12 chr8: 23,644,006-25,050,475	NKX2-6, RNU1-148P, 19 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	NKX2-6, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	NKX2-6, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	NKX2-6, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	NKX2-6, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	NKX2-6, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	NKX2-6, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	NKX2-6, LOC105375890, 2105 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 77

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Number of Variants: 20

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