dbVar for Gene (Select 91746) - 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
nsv7147679	copy number variation	1	nstd232	human		GRCh37.p13 chr4: 69,195,836-69,195,917 , GRCh38.p12 chr4: 68,330,118-68,330,199	YTHDC1
nsv7137327	insertion	1	nstd232	human		GRCh37.p13 chr4: 69,203,618-69,203,618 , GRCh38.p12 chr4: 68,337,900-68,337,900	YTHDC1
nsv6757154	copy number variation	1	nstd229	human		GRCh38 chr4: 68,260,292-68,462,221 , GRCh37.p13 chr4: 69,126,010-69,327,939	APOOP4, YTHDC1, 3 more genes
nsv6752823	copy number variation	1	nstd229	human		GRCh38 chr4: 68,311,784-68,311,964 , GRCh37.p13 chr4: 69,177,502-69,177,682	YTHDC1
nsv6752054	copy number variation	1	nstd229	human		GRCh38 chr4: 68,291,201-68,327,600 , GRCh37.p13 chr4: 69,156,919-69,193,318	APOOP4, YTHDC1, 1 more genes
nsv6742302	copy number variation	1	nstd229	human		GRCh38 chr4: 68,322,301-68,327,600 , GRCh37.p13 chr4: 69,188,019-69,193,318	YTHDC1
nsv6636262	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 68,918,505-69,181,506 , GRCh38.p12 chr4: 68,052,787-68,315,788	LOC100420693, SYT14P1, 8 more genes
nsv6557680	inversion	1	nstd223	human		GRCh38 chr4: 68,326,742-68,327,229 , GRCh37.p13 chr4: 69,192,460-69,192,947	YTHDC1
nsv6392511	copy number variation	1	nstd223	human		GRCh38 chr4: 68,332,101-68,333,800 , GRCh37.p13 chr4: 69,197,819-69,199,518	YTHDC1
nsv6391190	copy number variation	1	nstd223	human		GRCh38 chr4: 68,330,147-68,330,649 , GRCh37.p13 chr4: 69,195,865-69,196,367	YTHDC1
nsv6388522	copy number variation	1	nstd223	human		GRCh38 chr4: 68,339,901-68,341,500 , GRCh37.p13 chr4: 69,205,619-69,207,218	YTHDC1
nsv6388344	copy number variation	1	nstd223	human		GRCh38 chr4: 68,319,338-68,320,041 , GRCh37.p13 chr4: 69,185,056-69,185,759	YTHDC1
nsv6379623	copy number variation	1	nstd223	human		GRCh38 chr4: 68,308,589-68,308,935 , GRCh37.p13 chr4: 69,174,307-69,174,653	YTHDC1
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
nsv6313740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800	CXCL8, UGT2A1, 175 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	SNHG27, TNIP3, 1091 more genes
nsv6244200	mobile element insertion	1	nstd215	human		GRCh38 chr4: 68,336,901-68,336,901 , GRCh37.p13 chr4: 69,202,619-69,202,619	YTHDC1
nsv6244199	mobile element insertion	1	nstd215	human		GRCh38 chr4: 68,327,971-68,327,971 , GRCh37.p13 chr4: 69,193,689-69,193,689	YTHDC1
nsv6137861	copy number variation	1	nstd102	human	association	GRCh37 chr4: 68,871,643-69,625,838 , GRCh38.p12 chr4: 68,005,925-68,760,120	MTND2P41, APOOP4, 19 more genes
nsv6135602	copy number variation	1	nstd213	human		GRCh37 chr4: 69,150,000-69,260,001 , GRCh38.p12 chr4: 68,284,282-68,394,283	MT2P1, YTHDC1, 2 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

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Links from Gene

Items: 1 to 20 of 241

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Number of Variants: 20

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