mal2[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3901895	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr8: 120,252,409-120,270,739 , GRCh38.p12 chr8: 119,240,169-119,258,499	MAL2, MAL2-AS1
nsv3916342	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr8: 119,196,262-119,291,664 , NCBI36 chr8: 120,277,682-120,373,085 , GRCh37 chr8: 120,208,501-120,303,904	MAL2, LOC105375725, 1 more genes
nsv3921960	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr8: 120,154,493-120,372,683 , GRCh37.p13 chr8: 120,085,312-120,303,502 , GRCh38.p12 chr8: 119,073,073-119,291,262	MAL2, LOC105375725, 2 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	MAL2, 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	MAL2, 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	MAL2, 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	MAL2, 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	MAL2, 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	MAL2, LOC105375723, 93 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	MAL2, LOC107986968, 75 more genes
nsv7148124	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500	MAL2, LINC02964, 115 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	MAL2, 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	MAL2, 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	MAL2, UTP23, 65 more genes
nsv3924622	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 119,140,612-122,655,858 , GRCh38 chr8: 118,059,192-121,574,437 , GRCh37 chr8: 119,071,431-122,586,677	MAL2, LOC105375723, 35 more genes
nsv6637672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 118,645,068-121,684,174 , GRCh38.p12 chr8: 117,632,829-120,671,934	MAL2, RPS26P35, 34 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	MAL2, SAMD12, 38 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	MAL2, 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	MAL2, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	MAL2, LOC101929488, 2105 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:

Search results

Items: 1 to 20 of 59

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 59

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity