bcl7b[All Fields] AND 1[has_clinical] - 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
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	BCL7B, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	BCL7B, LOC107986817, 2014 more genes
nsv3917508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922	BCL7B, GTF2IP4, 285 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	BCL7B, GTF2IP1, 184 more genes
nsv3911276	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085	BCL7B, POM121, 155 more genes
nsv3914569	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 68,668,307-73,710,276 , NCBI36 chr7: 67,771,230-72,762,542 , GRCh37 chr7: 68,133,294-72,806,397	BCL7B, SPDYE7P, 61 more genes
nsv4729646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180	BCL7B, LOC105375346, 70 more genes
nsv4728820	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283	BCL7B, FDPSP7, 119 more genes
nsv3902539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,456,604-76,007,380 , GRCh38.p12 chr7: 72,986,074-76,378,063	BCL7B, WBSCR23, 97 more genes
nsv3922160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 72,404,249-76,189,514 , GRCh38 chr7: 73,352,304-76,722,261 , GRCh37 chr7: 72,766,313-76,351,578	BCL7B, PMS2P10, 88 more genes
nsv4675200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063	BCL7B, PHB1P15, 87 more genes
nsv4349368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,744,494-76,038,818 , GRCh38.p12 chr7: 73,330,491-76,409,501	BCL7B, MDH2, 83 more genes
nsv3912976	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 70,564,048-72,666,996 , GRCh38 chr7: 71,461,127-73,614,730 , GRCh37 chr7: 70,926,112-72,806,397	BCL7B, RNU6-1080P, 38 more genes
nsv3894940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,536,980-74,629,034 , GRCh38.p12 chr7: 73,122,656-75,175,451	BCL7B, TRIM50, 53 more genes
nsv6315397	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,589,515-74,629,034 , GRCh38.p12 chr7: 73,175,475-75,175,451	BCL7B, MIR10525, 52 more genes
nsv3892254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,612,042-74,574,641 , GRCh38.p12 chr7: 73,198,002-75,158,835	BCL7B, FZD9, 51 more genes
nsv3901656	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,305,671-74,196,360 , GRCh38.p12 chr7: 72,835,092-74,782,015	BCL7B, ELN, 58 more genes
nsv3922916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 72,930,548-74,869,255 , NCBI36 chr7: 72,039,022-73,923,281 , GRCh37 chr7: 72,401,086-74,285,345	BCL7B, VPS37D, 56 more genes
nsv3901730	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,589,515-74,386,749 , GRCh38.p12 chr7: 73,175,475-74,972,599	BCL7B, METTL27, 49 more genes
nsv3891763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,608,514-74,386,749 , GRCh38.p12 chr7: 73,194,474-74,972,599	BCL7B, CLDN3, 48 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

Additional filters

Search results

Items: 1 to 20 of 153

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Number of Variants: 20

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Search details

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