ash2l[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
nsv6637025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865	ASH2L, LINC02948, 185 more genes
nsv3918177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 29,362,097-40,231,708 , NCBI36 chr8: 29,275,533-40,208,384 , GRCh37 chr8: 29,219,614-40,089,227	ASH2L, RPL23P10, 159 more genes
nsv3919419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 34,169,768-43,014,044 , GRCh38 chr8: 34,312,250-43,158,901 , NCBI36 chr8: 34,289,310-43,133,201	ASH2L, PLEKHA2, 135 more genes
nsv3922311	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 37,428,611-47,058,107 , GRCh37.p13 chr8: 37,309,453-46,938,942 , GRCh38.p12 chr8: 37,451,935-46,027,320	ASH2L, CHRNB3, 120 more genes
nsv3924317	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 38,042,602-40,318,326 , GRCh38 chr8: 38,065,927-40,341,650 , GRCh37 chr8: 37,923,445-40,199,169	ASH2L, RPL3P10, 37 more genes
nsv6312909	copy number variation	5	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700	ASH2L, LSM1, 33 more genes
nsv3919682	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 38,023,037-39,148,929 , GRCh37 chr8: 37,903,880-39,029,772 , GRCh38 chr8: 38,046,362-39,172,253	ASH2L, RPL3P10, 24 more genes
nsv7148269	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 37,814,644-38,528,889 , GRCh37.p13 chr8: 37,672,162-38,386,407	ASH2L, GOT1L1, 20 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	ASH2L, 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	ASH2L, 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	ASH2L, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	ASH2L, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	ASH2L, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	ASH2L, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	ASH2L, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	ASH2L, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	ASH2L, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	ASH2L, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	ASH2L, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	ASH2L, LOC112268016, 1819 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 57

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 57

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity