clcn1[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
nsv4683443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,021,494-143,028,755 , GRCh38.p12 chr7: 143,324,401-143,331,662	CLCN1
nsv3888321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,042,594-143,047,767 , GRCh38 chr7: 143,345,501-143,350,674	CLCN1
nsv7097868	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,039,002-143,044,062 , GRCh38.p12 chr7: 143,341,909-143,346,969	CLCN1
nsv7097610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,013,350-143,018,251 , GRCh38.p12 chr7: 143,316,257-143,321,158	CLCN1
nsv5673925	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,316,257-143,321,158 , GRCh37 chr7: 143,013,350-143,018,251	CLCN1
nsv6312531	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,042,594-143,044,062 , GRCh38.p12 chr7: 143,345,501-143,346,969	CLCN1
nsv7097347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,027,845-143,028,765 , GRCh38.p12 chr7: 143,330,752-143,331,672	CLCN1
nsv6312530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,013,209-143,049,107 , GRCh38.p12 chr7: 143,316,116-143,352,014	CLCN1, FAM131B
nsv6312435	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 143,013,306-143,049,058 , GRCh38.p12 chr7: 143,316,213-143,351,965	CLCN1, FAM131B
nsv4450468	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 143,047,445-143,049,078 , GRCh38 chr7: 143,350,352-143,351,985	CLCN1, FAM131B
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	CLCN1, RNU6-438P, 2682 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	CLCN1, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	CLCN1, MOXD2P, 561 more genes
nsv3897512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017	CLCN1, LOC105375548, 520 more genes
nsv7097864	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 130,781,014-150,301,047 , GRCh38.p12 chr7: 131,096,255-150,603,959	CLCN1, NOBOX, 466 more genes
nsv3903590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080	CLCN1, LOC105375597, 468 more genes
nsv3910344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973	CLCN1, LOC112268012, 461 more genes
nsv3905379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017	CLCN1, AGAP3, 459 more genes
nsv3919772	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866	CLCN1, LOC105375567, 429 more genes
nsv6636458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,779,213-149,042,734 , GRCh38.p12 chr7: 132,094,454-149,345,643	CLCN1, TRBD2, 403 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

Search results

Items: 1 to 20 of 56

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Number of Variants: 20

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