rpl3l[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
nsv3898566	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 1,991,251-1,997,211 , GRCh38.p12 chr16: 1,941,250-1,947,210	RPL3L, MSRB1
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	RPL3L, JPT2, 128 more genes
nsv3919589	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582	RPL3L, C1QTNF8, 127 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	RPL3L, MRPS34, 102 more genes
nsv4449893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655	RPL3L, LMF1-AS1, 99 more genes
nsv7098880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378	RPL3L, TPSP1, 78 more genes
nsv4683209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709	RPL3L, TMEM204, 67 more genes
nsv3893007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,734,363-2,285,561 , GRCh38.p12 chr16: 1,684,362-2,235,560	RPL3L, IGFALS, 49 more genes
nsv4682253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,573,499-2,114,448 , GRCh38.p12 chr16: 1,523,498-2,064,447	RPL3L, NHERF2, 37 more genes
nsv6289860	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 1,851,807-2,093,151 , GRCh37.p13 chr16: 1,901,808-2,143,152	RPL3L, HS3ST6, 24 more genes
nsv6315059	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 1,903,155-2,093,402 , GRCh37.p13 chr16: 1,953,156-2,143,403	RPL3L, NPW, 21 more genes
nsv6309997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,003,468-2,126,543 , GRCh38.p12 chr16: 1,953,467-2,076,542	RPL3L, NHERF2, 16 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	RPL3L, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	RPL3L, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	RPL3L, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	RPL3L, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	RPL3L, FTLP14, 1868 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	RPL3L, BMERB1, 701 more genes
nsv3903116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686	RPL3L, NPIPA8, 616 more genes
nsv3900978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599	RPL3L, LOC105371091, 543 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 55

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 55

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity