h3c8[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
nsv6290728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 26,008,259-26,168,230 , GRCh38.p12 chr6: 26,008,031-26,168,002	H2BC3, H1-1, 18 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	H3C8, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	H3C8, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	H3C8, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	H3C8, ITPR3, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	H3C8, TRR-ACG1-2, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	H3C8, PRELID1P2, 785 more genes
nsv4675352	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 26,238,509-26,329,714 , GRCh38.p12 chr6: 26,238,281-26,329,486	H3C8, H3C9P, 22 more genes
nsv3877272	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,609,423-28,016,099 , GRCh38.p12 chr6: 27,641,644-28,048,321	HCG13P, H2AC13, 47 more genes
nsv4675044	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 27,616,157-28,011,557 , GRCh38.p12 chr6: 27,648,378-28,043,779	H2BC16P, H2BC17, 46 more genes
nsv3920471	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 25,991,630-26,280,921 , NCBI36 chr6: 26,099,609-26,388,900 , GRCh38 chr6: 25,991,402-26,280,693	H3C8, H2AC8, 41 more genes
nsv3885670	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,645,278-27,902,992 , GRCh38.p12 chr6: 27,677,499-27,935,214	H2AC16, RNU7-26P, 35 more genes
nsv3871028	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 26,110,314-26,338,056 , GRCh38.p12 chr6: 26,110,086-26,337,828	H3C8, LOC101928743, 41 more genes
nsv3874106	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,715,243-27,890,631 , GRCh38.p12 chr6: 27,747,464-27,922,853	H3C11, H2BC14, 27 more genes
nsv3873271	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,710,165-27,885,437 , GRCh38.p12 chr6: 27,742,386-27,917,659	TRX-CAT1-7, RNU7-26P, 27 more genes
nsv3874998	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,715,470-27,886,830 , GRCh38.p12 chr6: 27,747,691-27,919,052	LOC100131289, H3C12, 27 more genes
nsv3884368	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,715,243-27,877,446 , GRCh38.p12 chr6: 27,747,464-27,909,668	TRX-CAT1-7, H2AC17, 27 more genes
nsv3881488	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,713,299-27,872,832 , GRCh38.p12 chr6: 27,745,520-27,905,054	H4C10P, H3C10, 26 more genes
nsv3878745	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 27,715,243-27,871,553 , GRCh38.p12 chr6: 27,747,464-27,903,775	LOC100131289, H2AC14, 26 more genes
nsv3918212	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 25,991,619-26,117,057 , GRCh38 chr6: 25,991,391-26,116,829 , NCBI36 chr6: 26,099,598-26,225,036	H2AC4, H4C2, 14 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 38

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Number of Variants: 20

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