dbVar for Nucleotide (Select 303308501) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv6121552	copy number variation	1	nstd186	human	GRCh37 chr16: 69,191,808-69,192,074 , GRCh38.p12 chr16\|NW_003315946.1: 71,652-71,918 , GRCh38.p12 chr16: 69,157,905-69,158,171	UTP4
nsv4857539	copy number variation	1	nstd200	human	GRCh37 chr16: 69,242,943-69,245,937 , GRCh38.p12 chr16: 69,209,040-69,212,034 , GRCh38.p12 chr16\|NW_003315946.1: 12,657-15,651	SNTB2
nsv4857538	copy number variation	1	nstd200	human	GRCh37 chr16: 69,226,855-69,227,756 , GRCh38.p12 chr16\|NW_003315946.1: 30,838-31,739 , GRCh38.p12 chr16: 69,192,952-69,193,853	SNTB2
nsv4857537	copy number variation	1	nstd200	human	GRCh37 chr16: 69,211,807-69,215,622 , GRCh38.p12 chr16: 69,177,904-69,181,719 , GRCh38.p12 chr16\|NW_003315946.1: 48,111-51,928	0
nsv4857536	copy number variation	1	nstd200	human	GRCh37 chr16: 69,211,179-69,212,989 , GRCh38.p12 chr16\|NW_003315946.1: 50,744-52,556 , GRCh38.p12 chr16: 69,177,276-69,179,086	RNU6-22P
nsv4857535	copy number variation	1	nstd200	human	GRCh37 chr16: 69,209,323-69,210,355 , GRCh38.p12 chr16\|NW_003315946.1: 53,380-54,412 , GRCh38.p12 chr16: 69,175,420-69,176,452	RNU6-22P
nsv4786106	mobile element deletion	1	nstd200	human	GRCh37 chr16: 69,195,867-69,196,150 , GRCh38.p12 chr16\|NW_003315946.1: 67,575-67,858 , GRCh38.p12 chr16: 69,161,964-69,162,247	UTP4
nsv4760259	insertion	1	nstd199	human	GRCh37 chr16: 69,191,801-69,191,801 , GRCh38.p12 chr16\|NW_003315946.1: 71,925-71,925 , GRCh38.p12 chr16: 69,157,898-69,157,898	UTP4
nsv4759880	insertion	1	nstd199	human	GRCh37 chr16: 69,241,849-69,241,849 , GRCh38.p12 chr16: 69,207,946-69,207,946 , GRCh38.p12 chr16\|NW_003315946.1: 16,745-16,745	SNTB2
nsv4743370	copy number variation	1	nstd199	human	GRCh37 chr16: 69,240,456-69,240,520 , GRCh38.p12 chr16\|NW_003315946.1: 18,074-18,138 , GRCh38.p12 chr16: 69,206,553-69,206,617	SNTB2
nsv4719841	insertion	1	nstd186	human	GRCh37 chr16: 69,191,794-69,191,794 , GRCh38.p12 chr16: 69,157,891-69,157,891 , GRCh38.p12 chr16\|NW_003315946.1: 71,932-71,932	UTP4
nsv4634434	copy number variation	1	nstd186	human	GRCh37 chr16: 69,191,808-69,192,062 , GRCh38.p12 chr16: 69,157,905-69,158,159 , GRCh38.p12 chr16\|NW_003315946.1: 71,664-71,918	UTP4
nsv4633015	copy number variation	1	nstd183	human	GRCh37 chr16: 69,220,993-69,221,884 , GRCh38.p12 chr16\|NW_003315946.1: 41,849-42,740 , GRCh38.p12 chr16: 69,187,090-69,187,981	SNTB2
nsv4539057	insertion	1	nstd166	human	GRCh37.p13 chr16: 69,191,794-69,191,794 , GRCh38.p12 chr16: 69,157,891-69,157,891 , GRCh38.p12 chr16\|NW_003315946.1: 71,932-71,932	UTP4
nsv4531869	copy number variation	1	nstd166	human	GRCh37.p13 chr16: 69,236,180-69,236,315 , GRCh38.p12 chr16\|NW_003315946.1: 22,279-22,414 , GRCh38.p12 chr16: 69,202,277-69,202,412	SNTB2
nsv4530852	copy number variation	1	nstd166	human	GRCh37.p13 chr16: 69,191,808-69,192,062 , GRCh38.p12 chr16\|NW_003315946.1: 71,664-71,918 , GRCh38.p12 chr16: 69,157,905-69,158,159	UTP4
nsv4438436	insertion	1	nstd175	human	GRCh37 chr16: 69,191,805-69,191,805 , GRCh38.p12 chr16: 69,157,902-69,157,902 , GRCh38.p12 chr16\|NW_003315946.1: 71,921-71,921	UTP4
nsv4371382	copy number variation	1	nstd173	human	GRCh37 chr16: 69,162,105-69,206,045 , GRCh38.p12 chr16: 69,128,202-69,172,142 , GRCh38.p12 chr16\|NW_003315946.1: 57,690-89,672	UTP4, CHTF8, 1 more genes
nsv4250009	copy number variation	1	nstd166	human	GRCh37.p13 chr16: 69,241,313-69,254,360 , GRCh38.p12 chr16: 69,207,410-69,220,457 , GRCh38.p12 chr16\|NW_003315946.1: 4,234-17,281	SNTB2
nsv4249212	copy number variation	1	nstd166	human	GRCh37.p13 chr16: 69,193,829-69,193,947 , GRCh38.p12 chr16\|NW_003315946.1: 69,778-69,897 , GRCh38.p12 chr16: 69,159,926-69,160,044	UTP4

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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

Links from Nucleotide

Items: 1 to 20 of 208

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Number of Variants: 20

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Supplemental Content

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