dbVar for Gene (Select 5981) - 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
nsv7148229	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249	LINC01587, RN7SKP82, 509 more genes
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	OR7E84P, FAM193A, 764 more genes
nsv7145857	insertion	1	nstd232	human		GRCh37.p13 chr4: 39,313,168-39,313,168 , GRCh38.p12 chr4: 39,311,548-39,311,548	RFC1
nsv7098857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 39,245,868-39,700,010 , GRCh38.p12 chr4: 39,244,248-39,698,390	UGDH, UBE2K, 13 more genes
nsv7097249	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 39,187,326-39,478,735 , GRCh38.p12 chr4: 39,185,706-39,477,115	RNU6-32P, RNU6-887P, 6 more genes
nsv7096849	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 38,765,721-39,478,735 , GRCh38.p12 chr4: 38,764,100-39,477,115	TMEM156, TLR6, 14 more genes
nsv7052968	inversion	1	nstd229	human		GRCh38 chr4: 39,356,015-39,356,082 , GRCh37.p13 chr4: 39,357,635-39,357,702	RFC1
nsv7049186	inversion	1	nstd229	human		GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929	SMIM14, RNU6-887P, 42 more genes
nsv7038584	inversion	1	nstd229	human		GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525	RPL9, UBE2K, 41 more genes
nsv6735357	copy number variation	1	nstd229	human		GRCh38 chr4: 39,342,201-39,389,600 , GRCh37.p13 chr4: 39,343,821-39,391,220	RFC1
nsv6734359	copy number variation	1	nstd229	human		GRCh38 chr4: 39,230,901-39,308,100 , GRCh37.p13 chr4: 39,232,521-39,309,720	RFC1, RNU6-32P, 1 more genes
nsv6734095	copy number variation	1	nstd229	human		GRCh38 chr4: 39,343,012-39,343,351 , GRCh37.p13 chr4: 39,344,632-39,344,971	RFC1
nsv6734066	copy number variation	1	nstd229	human		GRCh38 chr4: 39,292,592-39,293,314 , GRCh37.p13 chr4: 39,294,212-39,294,934	RFC1
nsv6733652	copy number variation	1	nstd229	human		GRCh38 chr4: 39,332,226-39,341,504 , GRCh37.p13 chr4: 39,333,846-39,343,124	RFC1
nsv6732844	copy number variation	1	nstd229	human		GRCh38 chr4: 39,309,214-39,310,719 , GRCh37.p13 chr4: 39,310,834-39,312,339	RFC1
nsv6732169	copy number variation	1	nstd229	human		GRCh38 chr4: 39,256,701-39,308,800 , GRCh37.p13 chr4: 39,258,321-39,310,420	WDR19, RFC1, 1 more genes
nsv6731771	copy number variation	1	nstd229	human		GRCh38 chr4: 39,033,924-39,356,182 , GRCh37.p13 chr4: 39,035,544-39,357,802	RFC1, LOC105374418, 3 more genes
nsv6730540	copy number variation	1	nstd229	human		GRCh38 chr4: 39,346,515-39,351,343 , GRCh37.p13 chr4: 39,348,135-39,352,963	RFC1
nsv6727045	copy number variation	1	nstd229	human		GRCh38 chr4: 39,286,031-39,286,099 , GRCh37.p13 chr4: 39,287,651-39,287,719	RFC1, WDR19

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Number of Variants: 20

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Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 368

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Number of Variants: 20

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