rad21[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
nsv4682931	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 117,869,506-117,875,498 , GRCh38.p12 chr8: 116,857,267-116,863,259	RAD21
nsv6634633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 117,860,986-117,861,652 , GRCh38 chr8: 116,848,747-116,849,413	RAD21
nsv3890696	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 117,845,995-117,878,859 , GRCh38.p12 chr8: 116,833,756-116,866,620	RAD21
nsv6312389	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 117,859,739-117,866,727 , GRCh38.p12 chr8: 116,847,500-116,854,488	RAD21
nsv3890871	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 117,649,533-117,863,721 , GRCh38.p12 chr8: 116,637,294-116,851,482	RAD21, UTP23, 3 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	RAD21, RNU4-37P, 220 more genes
nsv3876297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 114,508,086-129,040,004 , GRCh38.p12 chr8: 113,495,857-128,027,758	RAD21, ZHX1-C8orf76, 172 more genes
nsv3901450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 107,032,887-120,742,018 , GRCh38.p12 chr8: 106,020,659-119,729,778	RAD21, AARD, 112 more genes
nsv3914003	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 114,369,859-127,797,514 , GRCh38 chr8: 113,288,454-126,716,087 , GRCh37 chr8: 114,300,683-127,728,332	RAD21, RNU6-442P, 154 more genes
nsv3904565	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 110,250,943-123,515,785 , GRCh38.p12 chr8: 109,238,714-122,503,546	RAD21, TAF2, 108 more genes
nsv4675222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 111,514,791-123,192,373 , GRCh38.p12 chr8: 110,502,562-122,180,134	RAD21, LOC105375723, 93 more genes
nsv3891444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 111,137,305-119,897,611 , GRCh38.p12 chr8: 110,125,076-118,885,372	RAD21, LOC105375712, 58 more genes
nsv3917391	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 115,014,710-123,703,161 , GRCh37 chr8: 114,945,534-123,633,980 , GRCh38 chr8: 113,933,305-122,621,741	RAD21, LOC107986968, 75 more genes
nsv3923146	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 114,560,780-122,594,102 , NCBI36 chr8: 115,642,185-123,675,522 , GRCh37 chr8: 115,573,009-123,606,341	RAD21, LOC105375721, 73 more genes
nsv3920453	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 113,418,060-120,975,305 , GRCh37 chr8: 114,430,289-121,987,545 , NCBI36 chr8: 114,499,465-122,056,726	RAD21, LOC102723447, 67 more genes
nsv3910425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 113,540,571-121,095,280 , GRCh38 chr8: 112,528,342-120,083,041 , NCBI36 chr8: 113,609,747-121,164,461	RAD21, UTP23, 65 more genes
nsv7097416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 117,859,739-120,844,804 , GRCh38.p12 chr8: 116,847,500-119,832,564	RAD21, SAMD12, 38 more genes
nsv3900134	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 117,714,768-119,072,307 , GRCh38.p12 chr8: 116,702,529-118,060,068	RAD21, LOC107986970, 18 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	RAD21, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	RAD21, TBC1D31, 2109 more genes

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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 62

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Number of Variants: 20

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Supplemental Content

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Search details

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