c7[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
nsv6311765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 40,947,684-40,950,136 , GRCh38.p12 chr5: 40,947,582-40,950,034	C7
nsv7096775	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 40,921,002-40,936,566 , GRCh38.p12 chr5: 40,920,900-40,936,464	C7
nsv6312106	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 40,928,662-40,937,812 , GRCh38.p12 chr5: 40,928,560-40,937,710	C7
nsv4675150	copy number variation	2	nstd102	human	Uncertain significance, Likely benign	GRCh37 chr5: 40,876,451-41,007,848 , GRCh38.p12 chr5: 40,876,349-41,007,746	C7, MROH2B, 1 more genes
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	C7, MEGF10, 2080 more genes
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	EREG, EFL1P2, 530 more genes
nsv4729598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632	PTPN11P5, LOC643014, 244 more genes
nsv6314916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218	MICOS10P4, SULT1B1, 274 more genes
nsv4674589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079	SOWAHB, FTLP9, 211 more genes
nsv4674141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444	COX18, UGT2B11, 216 more genes
nsv3922666	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 76,597,345-85,234,472 , GRCh38 chr4: 75,453,111-84,094,295 , GRCh37 chr4: 76,378,321-85,015,448	LOC100421142, HIGD1AP13, 146 more genes
nsv6313715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000	CCNG2, FTLP9, 129 more genes
nsv4456138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,561,780-78,304,341 , GRCh38.p12 chr4: 70,696,063-77,383,187	ANKRD17-DT, LOC643014, 119 more genes
nsv4674327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933	GP1BB, DGCR11, 308 more genes
nsv3917936	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 18,659,766-22,152,986 , GRCh38 chr22: 18,339,130-23,480,799 , GRCh37 chr22: 20,279,766-23,822,986	IGLV7-46, FAM230F, 298 more genes
nsv3916402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,081,260-24,593,820 , NCBI36 chr22: 19,411,260-22,923,820 , GRCh38 chr22: 20,726,972-24,197,852	FAM247A, IGLV1-36, 221 more genes
nsv3897974	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-24,885,806 , GRCh38.p12 chr22: 21,111,372-24,489,838	IGLV2-34, ZDHHC8BP, 214 more genes
nsv3892419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,749,625-23,972,878 , GRCh38.p12 chr22: 20,395,335-23,630,691	KRT18P5, SLC9A3P2, 217 more genes
nsv3901484	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,465,661-24,653,491 , GRCh38.p12 chr22: 21,111,372-24,257,523	PCAT14, CHCHD10, 208 more genes
nsv3904613	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 20,716,876-23,819,697 , GRCh38.p12 chr22: 20,362,586-23,477,510	LL22NC03-102D1.18, IGLL5, 212 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 180

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Number of Variants: 20

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