xkr6[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
nsv6315449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940	XKR6, 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	XKR6, 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	XKR6, ENTPD4, 447 more genes
nsv6636968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205	XKR6, ZNF705B, 357 more genes
nsv4455719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213	XKR6, MIR598, 312 more genes
nsv4685988	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110	XKR6, ZNF705B, 232 more genes
nsv7148131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120	XKR6, FAM90A11, 224 more genes
nsv6634376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-11,281,408 , GRCh38.p12 chr8: 208,048-11,423,899	XKR6, DLGAP2-AS1, 228 more genes
nsv6636940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117	XKR6, HSPD1P3, 270 more genes
nsv3902717	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-10,939,681 , GRCh38.p12 chr8: 208,048-11,082,171 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617	XKR6, LOC101929128, 270 more genes
nsv3900231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-10,197,718 , GRCh38.p12 chr8\|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 60,213-10,340,208	XKR6, LOC105377793, 273 more genes
nsv3916160	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 3,791,727-11,384,448 , GRCh38 chr8: 3,934,205-11,526,939 , NCBI36 chr8: 3,779,135-11,421,857	XKR6, DEFB109B, 189 more genes
nsv3914458	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 7,079,769-12,416,695 , GRCh38 chr8: 7,234,837-12,514,815 , GRCh37 chr8: 7,092,359-12,372,324	XKR6, DEFB103B, 191 more genes
nsv3917857	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 7,040,596-12,285,523 , GRCh38 chr8: 7,195,664-12,383,643 , GRCh37 chr8: 7,053,186-12,241,152	XKR6, MIR124-1, 185 more genes
nsv3916612	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 7,256,229-11,843,369 , GRCh37.p13 chr8: 7,268,819-11,805,960 , GRCh38.p12 chr8: 7,411,297-11,948,451 , GRCh38.p12 chr8\|NW_018654717.1: 655,251-5,419,355	XKR6, DEFB107A, 167 more genes
nsv3912043	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 7,411,297-11,961,807 , NCBI36 chr8: 7,256,229-11,856,725 , GRCh37 chr8: 7,268,819-11,819,316	XKR6, LOC105379241, 138 more genes
nsv6636617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 8,093,066-12,548,732 , GRCh38.p12 chr8: 8,235,544-12,691,223 , GRCh38.p12 chr8\|NW_018654717.1: 996,517-5,112,321	XKR6, DEFB131D, 128 more genes
nsv3918988	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 8,148,437-12,511,914 , GRCh38 chr8: 8,253,505-12,610,034 , GRCh37 chr8: 8,111,027-12,467,543	XKR6, LOC649352, 118 more genes
nsv3915937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 8,130,630-12,467,543 , GRCh38 chr8: 8,273,108-12,610,034 , NCBI36 chr8: 8,168,040-12,511,914	XKR6, DEFB109E, 118 more genes
nsv3914682	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 8,079,861-12,241,152 , NCBI36 chr8: 8,117,271-12,285,523 , GRCh38 chr8: 8,222,339-12,383,643	XKR6, FAM66D, 112 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 124

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Number of Variants: 20

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