dbVar for Gene (Select 255167) - 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
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	OTULINL, AKTIPP2, 317 more genes
nsv5041416	inversion	1	nstd200	human		GRCh38 chr5: 6,583,518-8,812,732 , GRCh37.p13 chr5: 6,583,631-8,812,844	RNA5SP176, MTND6P2, 36 more genes
nsv4685752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860	LINC01377, LOC100421308, 277 more genes
nsv4674497	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071	LOC101929003, MTCYBP37, 192 more genes
nsv4674444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432	LOC100132773, LINC01019, 125 more genes
nsv4674161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267	LOC102723561, LOC107986397, 287 more genes
nsv4674130	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608	SLC9A3-AS1, LINC02114, 169 more genes
nsv4456747	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 5,499,308-6,666,236 , GRCh38.p12 chr5: 5,499,195-6,666,123	MED10, UBE2QL1, 8 more genes
nsv4369315	copy number variation	1	nstd173	human		GRCh37 chr5: 113,577-10,304,966 , GRCh38.p12 chr5: 113,462-10,304,854	, LOC105374625, 158 more genes
nsv4349271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 140,474-26,906,925 , GRCh38.p12 chr5: 140,359-26,906,816	MIR4636, LRRC14B, 304 more genes
nsv4348815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 140,474-9,792,158 , GRCh38.p12 chr5: 140,359-9,792,046	MIR4458HG, LOC100310782, 146 more genes
nsv3968600	complex substitution	1	nstd168	human		GRCh38 chr5: 6,565,551-6,586,200 , GRCh37.p13 chr5: 6,565,664-6,586,313	LINC01018
nsv3957601	insertion	1	nstd168	human		GRCh38 chr5: 6,545,434-6,586,200 , GRCh37.p13 chr5: 6,545,547-6,586,313	LINC01018
nsv3924736	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-33,454,051 , GRCh38 chr5: 22,149-33,418,188 , GRCh37 chr5: 22,149-33,418,294	LOC105374678, ZFR, 369 more genes
nsv3924496	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-32,248,116 , NCBI36 chr5: 75,149-32,283,873 , GRCh38 chr5: 22,149-32,248,010	LOC105374678, MIR4278, 356 more genes
nsv3923992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 50,093-46,115,086 , NCBI36 chr5: 103,093-46,150,843 , GRCh38 chr5: 49,978-46,114,984	LOC100130748, CDH10, 533 more genes
nsv3923869	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-7,266,388 , GRCh37 chr5: 22,149-7,213,388 , GRCh38 chr5: 22,149-7,213,275	CTD-2194D22.4, IRX2-DT, 113 more genes
nsv3923396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-27,188,057 , NCBI36 chr5: 75,149-27,223,814 , GRCh38 chr5: 22,149-27,187,950	LINC02899, TERLR1, 307 more genes
nsv3923129	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-16,584,575 , GRCh37 chr5: 22,149-16,584,684 , NCBI36 chr5: 75,149-16,637,684	AHRR, CTD-2154B17.1, 219 more genes
nsv3922865	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 22,149-28,429,241 , GRCh37 chr5: 22,149-28,429,348 , NCBI36 chr5: 75,149-28,465,105	CCT6P2, LOC105374661, 312 more genes

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 209

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Number of Variants: 20

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