dbVar for Gene (Select 55510) - 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
nsv7048284	inversion	1	nstd229	human		GRCh38 chr6: 73,272,579-75,940,581 , GRCh37.p13 chr6: 73,982,302-76,650,298	RPL39P3, KHDC1, 45 more genes
nsv6795537	copy number variation	1	nstd229	human		GRCh38 chr6: 73,413,171-73,413,207 , GRCh37.p13 chr6: 74,122,894-74,122,930	DDX43
nsv6793604	copy number variation	1	nstd229	human		GRCh38 chr6: 73,408,699-73,418,524 , GRCh37.p13 chr6: 74,118,422-74,128,247	DDX43
nsv6793244	copy number variation	1	nstd229	human		GRCh38 chr6: 73,407,412-73,507,729 , GRCh37.p13 chr6: 74,117,135-74,217,452	CGAS, RN7SL827P, 3 more genes
nsv6792901	copy number variation	1	nstd229	human		GRCh38 chr6: 73,401,101-73,427,936 , GRCh37.p13 chr6: 74,110,824-74,137,659	CGAS, DDX43
nsv6790487	copy number variation	1	nstd229	human		GRCh38 chr6: 73,006,301-73,863,300 , GRCh37.p13 chr6: 73,716,024-74,573,015	RBPMS2P1, SLC17A5, 24 more genes
nsv6787789	copy number variation	1	nstd229	human		GRCh38 chr6: 73,224,501-73,533,000 , GRCh37.p13 chr6: 73,934,224-74,242,723	DDX43, KHDC3L, 15 more genes
nsv6784485	copy number variation	1	nstd229	human		GRCh38 chr6: 73,256,414-73,487,243 , GRCh37.p13 chr6: 73,966,137-74,196,966	OOEP, RN7SL827P, 13 more genes
nsv6778682	copy number variation	1	nstd229	human		GRCh38 chr6: 73,416,201-73,423,000 , GRCh37.p13 chr6: 74,125,924-74,132,723	DDX43, CGAS
nsv6634377	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901	TXNP7, MTO1, 63 more genes
nsv6631323	copy number variation	1	nstd224	human		GRCh37 chr6: 74,115,413-74,135,255 , GRCh38.p12 chr6: 73,405,690-73,425,532	DDX43, CGAS
nsv6631322	copy number variation	1	nstd224	human		GRCh37 chr6: 74,072,466-74,541,452 , GRCh38.p12 chr6: 73,362,743-73,831,726	SLC17A5, KHDC3L, 12 more genes
nsv6573990	inversion	1	nstd223	human		GRCh38 chr6: 73,118,474-73,446,748 , GRCh37.p13 chr6: 73,828,197-74,156,471	DPPA5, EIF3EP1, 15 more genes
nsv6572827	inversion	1	nstd223	human		GRCh38 chr6: 73,401,792-73,402,857 , GRCh37.p13 chr6: 74,111,515-74,112,580	DDX43
nsv6570366	inversion	1	nstd223	human		GRCh38 chr6: 73,408,169-73,408,676 , GRCh37.p13 chr6: 74,117,892-74,118,399	DDX43
nsv6563328	inversion	1	nstd223	human		GRCh38 chr6: 73,409,956-73,410,434 , GRCh37.p13 chr6: 74,119,679-74,120,157	DDX43
nsv6559734	inversion	1	nstd223	human		GRCh38 chr6: 66,921,420-73,446,758 , GRCh37.p13 chr6: 67,631,313-74,156,481	RNA5SP208, KCNQ5, 72 more genes
nsv6413342	copy number variation	1	nstd223	human		GRCh38 chr6: 73,392,868-73,399,185 , GRCh37.p13 chr6: 74,102,591-74,108,908	DDX43
nsv6315402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961	LOC105377841, RPS6P8, 139 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	LOC101928570, RNU4-72P, 288 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

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Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 185

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Number of Variants: 20

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