dbVar for Gene (Select 128077) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7148149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 145,822,587-146,064,587 , GRCh37.p13 chr1\|NW_003871055.3: 2,638,000-2,880,000 , GRCh37.p13 chr1: 145,370,415-145,612,526	TXNIP, PEX11B, 22 more genes
nsv7148064	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,365,275-145,826,979 , GRCh38.p12 chr1: 145,608,084-146,069,727	ANKRD34A, RNVU1-6, 26 more genes
nsv7148054	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 142,535,935-157,648,813 , GRCh38.p12 chr1: 120,175,847-149,601,750	, TRN-GTT12-1, 266 more genes
nsv7137200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,382,123-145,792,051 , GRCh38.p12 chr1: 145,642,989-146,052,881	PDZK1, LOC107985593, 24 more genes
nsv7099228	copy number variation	1	nstd231	human		GRCh38.p12 chr1: 145,741,225-146,028,213 , GRCh37 chr1: 145,406,788-145,693,862	ITGA10, PEX11B, 15 more genes
nsv7098839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123	CCT8P1, LINC01719, 120 more genes
nsv7098747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,414,780-145,826,931 , GRCh38.p12 chr1: 145,608,132-146,020,233	TXNIP, CD160, 19 more genes
nsv7098724	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,397,357-148,344,744 , GRCh38.p12 chr1: 144,536,526-148,549,211	, LOC105371217, 150 more genes
nsv7056211	inversion	1	nstd229	human		GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1\|NW_003871055.3: 697,113-7,283,150	, PDIA3P1, 333 more genes
nsv7053757	inversion	1	nstd229	human		GRCh38 chr1: 145,861,640-146,012,316 , GRCh37.p13 chr1\|NW_003871055.3: 2,677,053-2,827,729 , GRCh37.p13 chr1: 145,422,688-145,573,428	RBM8A, LIX1L-AS1, 9 more genes
nsv7045394	inversion	1	nstd229	human		GRCh38 chr1: 143,732,174-147,339,264 , GRCh37.p13 chr1\|NW_003871055.3: 547,587-4,154,677	, MIR6736, 130 more genes
nsv7045117	inversion	1	nstd229	human		GRCh38 chr1: 143,671,956-145,963,983 , GRCh37.p13 chr1\|NW_003871055.3: 487,369-2,779,396	, GPR89A, 96 more genes
nsv6641625	copy number variation	1	nstd229	human		GRCh38 chr1: 145,931,569-145,978,371 , GRCh37.p13 chr1\|NW_003871055.3: 2,746,982-2,793,784 , GRCh37.p13 chr1: 145,456,713-145,503,524	ANKRD34A, LIX1L, 2 more genes
nsv6641568	copy number variation	1	nstd229	human		GRCh38 chr1: 145,931,397-145,935,003 , GRCh37.p13 chr1\|NW_003871055.3: 2,746,810-2,750,416 , GRCh37.p13 chr1: 145,500,085-145,503,696	LIX1L, LIX1L-AS1
nsv6641566	copy number variation	1	nstd229	human		GRCh38 chr1: 145,796,670-146,049,420 , GRCh37.p13 chr1\|NW_003871055.3: 2,612,083-2,864,833 , GRCh37.p13 chr1: 145,385,582-145,638,408	ANKRD34A, RNF115, 19 more genes
nsv6641458	copy number variation	1	nstd229	human		GRCh38 chr1: 145,834,456-145,939,172 , GRCh37.p13 chr1: 145,495,920-145,600,656 , GRCh37.p13 chr1\|NW_003871055.3: 2,649,869-2,754,585	PEX11B, MIR6736, 10 more genes
nsv6636744	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,493,131-147,831,043 , GRCh38.p12 chr1: 145,430,980-148,358,916	PDZK1, ANKRD34A, 102 more genes
nsv6634386	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,626,685-147,597,284 , GRCh38.p12 chr1: 145,430,980-148,125,001	LOC391092, NBPF10, 84 more genes
nsv6634368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,387,023-145,764,679 , GRCh38.p12 chr1: 145,670,380-146,047,980	TRK-CTT2-1, TXNIP, 22 more genes
nsv6634349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442	, TRN-GTT10-1, 170 more genes

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

Send to:

Links from Gene

Items: 1 to 20 of 640

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Recent activity

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 Gene

Items: 1 to 20 of 640

Page of 32

Number of Variants: 20

Page of 32

Supplemental Content

Find related data

Recent activity