gclc[All Fields] AND 1[has_clinical] - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3923721	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801	GCLC, PAQR8, 131 more genes
nsv3922315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788	GCLC, MLIP-AS1, 100 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	GCLC, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	GCLC, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	GCLC, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	GCLC, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	GCLC, HLA-DPB2, 1001 more genes
nsv3910455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 51,061,467-53,724,432 , GRCh38 chr6: 51,093,754-53,859,634 , NCBI36 chr6: 51,169,426-53,832,391	GCLC, LOC101927082, 58 more genes
nsv4729270	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747	GCLC, CRISP1, 105 more genes
nsv6314749	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313	GCLC, ACTG1P9, 245 more genes
nsv6638066	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706	GCLC, NPM1P36, 73 more genes
nsv4456287	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 53,113,873-53,385,343 , GRCh38.p12 chr6: 53,249,075-53,520,545	GCLC, RPS16P5, 9 more genes
nsv4729393	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 52,657,712-53,622,715 , GRCh38.p12 chr6: 52,792,914-53,757,917	GCLC, KILH, 29 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

gclc[All Fields] AND 1[has_clinical] (14)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)