2-1235-004 AND nstd173 - dbVar - NCBI

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

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4386852	copy number variation	127	nstd173	human		GRCh37 chr8: 137,677,896-137,862,435 , GRCh38.p12 chr8: 136,665,653-136,850,192	LINC02055
nsv4387797	copy number variation	78	nstd173	human		GRCh37 chr1: 72,773,260-72,812,440 , GRCh38.p12 chr1: 72,307,577-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-67,982	LOC105378797
nsv4379036	copy number variation	1	nstd173	human		GRCh37 chr1: 45,626,182-45,652,229 , GRCh38.p12 chr1: 45,160,510-45,186,557	ZSWIM5
nsv4368763	copy number variation	6	nstd173	human		GRCh37 chr22: 28,587,121-28,607,657 , GRCh38.p12 chr22: 28,191,133-28,211,669	TTC28
nsv4377726	copy number variation	23	nstd173	human		GRCh37 chr6: 55,823,233-55,843,659 , GRCh38.p12 chr6: 55,958,435-55,978,861	LOC107986539
nsv4373295	copy number variation	124	nstd173	human		GRCh37 chr13: 69,248,299-69,268,719 , GRCh38.p12 chr13: 68,674,167-68,694,587	RN7SL761P
nsv4369997	copy number variation	60	nstd173	human		GRCh37 chr8: 39,246,772-39,388,766 , GRCh38.p12 chr8: 39,389,253-39,531,247	ADAM3A, ADAM5
nsv4376403	copy number variation	119	nstd173	human		GRCh37 chr19: 53,517,242-53,553,087 , GRCh38.p12 chr19: 53,013,989-53,049,834	ERVV-1, ERVV-2
nsv4374985	copy number variation	188	nstd173	human		GRCh37 chr14: 73,995,761-74,024,031 , GRCh38.p12 chr14: 73,529,057-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4379351	copy number variation	123	nstd173	human		GRCh37 chr19: 51,321,391-51,345,568 , GRCh38.p12 chr19: 50,818,135-50,842,312	LOC105372441, KLK1, 2 more genes
nsv4370796	copy number variation	34	nstd173	human		GRCh37 chr5: 180,375,290-180,430,789 , GRCh38.p12 chr5: 180,948,290-181,003,789	LOC100128762, TMEM69P2, 3 more genes
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4378846	copy number variation	1	nstd173	human		GRCh37 chrY: 22,287,686-22,466,082 , GRCh38.p12 chrY: 20,125,800-20,304,196	0
nsv4374879	copy number variation	3	nstd173	human		GRCh37 chr9: 11,988,678-12,091,322 , GRCh38.p12 chr9: 11,988,678-12,091,322	0
nsv4370779	copy number variation	156	nstd173	human		GRCh37 chr5: 8,702,522-8,750,244 , GRCh38.p12 chr5: 8,702,410-8,750,132	0
nsv4388092	copy number variation	1	nstd173	human		GRCh37 chr4: 151,668,146-152,071,875 , GRCh38.p12 chr4: 150,746,994-151,150,723	LRBA, RPS3A, 6 more genes
nsv4370601	copy number variation	60	nstd173	human		GRCh37 chr14: 106,525,299-106,667,035 , GRCh38.p12 chr14: 106,069,054-106,210,392 , GRCh38.p12 chr14\|NT_187600.1: 536,823-678,161	IGHVII-15-1, IGHV1-14, 17 more genes
nsv4377179	copy number variation	143	nstd173	human		GRCh37 chr3: 162,521,297-162,626,676 , GRCh38.p12 chr3: 162,803,509-162,908,888	0
nsv4379278	copy number variation	2	nstd173	human		GRCh37 chr15: 81,988,453-82,089,070 , GRCh38.p12 chr15: 81,696,112-81,796,729	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

2-1235-004 AND nstd173 (20)
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)