nkx2-5[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
nsv4681030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,659,276-172,672,303 , GRCh38.p12 chr5: 173,232,273-173,245,300	NKX2-5
nsv4682581	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,659,552-172,672,303 , GRCh38.p12 chr5: 173,232,549-173,245,300	NKX2-5
nsv7097521	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,659,748-172,666,091 , GRCh38.p12 chr5: 173,232,745-173,239,088	NKX2-5
nsv7096766	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,657,631-172,661,899 , GRCh38.p12 chr5: 173,230,628-173,234,896	NKX2-5
nsv3871726	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 173,232,104-173,235,312 , GRCh37 chr5: 172,659,107-172,662,315	NKX2-5
nsv997027	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr5: 172,659,107-172,662,315 , GRCh38.p12 chr5: 173,232,104-173,235,312	NKX2-5
nsv3889010	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 172,659,552-172,672,303 , GRCh38 chr5: 173,232,549-173,245,300	NKX2-5
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	NKX2-5, MEGF10, 2080 more genes
nsv3879307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 164,207,156-172,799,124 , GRCh38.p12 chr5: 164,780,150-173,372,121	NKX2-5, RN7SL339P, 113 more genes
nsv4578263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841	NKX2-5, LINC01187, 112 more genes
nsv3914710	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 172,961,091-175,054,665 , GRCh37 chr5: 172,388,094-174,481,668 , NCBI36 chr5: 172,320,700-174,414,274	NKX2-5, CDC42P5, 40 more genes
nsv3919616	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,203,801-173,769,972 , GRCh38 chr5: 172,776,798-174,342,969 , NCBI36 chr5: 172,136,407-173,702,578	NKX2-5, LINC02995, 33 more genes
nsv7097134	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 172,089,144-172,774,583 , GRCh38.p12 chr5: 172,662,141-173,347,580	NKX2-5, RNA5SP200, 22 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	NKX2-5, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	NKX2-5, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	NKX2-5, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	NKX2-5, PJA2, 1228 more genes
nsv6315448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788	NKX2-5, GRM6, 554 more genes
nsv3921182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758	NKX2-5, RN7SKP148, 553 more genes
nsv3885523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343	NKX2-5, WWC1, 446 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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