2-1526-003 AND nstd173 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4373645	copy number variation	3	nstd173	human		GRCh37 chr9: 11,765,254-11,913,005 , GRCh38.p12 chr9: 11,765,254-11,913,005	LOC101929446
nsv4385393	copy number variation	144	nstd173	human		GRCh37 chr2: 98,063,371-98,162,188 , GRCh38.p12 chr2: 97,490,656-97,545,725	ANKRD36B
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
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4381816	copy number variation	5	nstd173	human		GRCh37 chr21: 15,006,458-15,033,966 , GRCh38.p12 chr21: 13,634,137-13,661,645	MIR3118-1, POTED
nsv4376418	copy number variation	25	nstd173	human		GRCh37 chr12: 2,235,941-2,258,023 , GRCh38.p12 chr12: 2,126,775-2,148,857 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-491,001	LOC107984131, CACNA1C
nsv4388025	copy number variation	4	nstd173	human		GRCh37 chr15: 24,350,856-24,478,406 , GRCh38.p12 chr15: 24,105,709-24,233,259	LOC105370732, PWRN2, 1 more genes
nsv4386088	copy number variation	74	nstd173	human		GRCh37 chr12: 11,219,930-11,256,413 , GRCh38.p12 chr12: 11,067,331-11,103,814	PRH1, TAS2R43, 3 more genes
nsv4365715	copy number variation	8	nstd173	human		GRCh37 chr11: 55,374,176-55,435,179 , GRCh38.p12 chr11: 55,606,700-55,667,703	OR4P4, OR4S2, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4372679	copy number variation	125	nstd173	human		GRCh37 chr14: 74,001,111-74,029,899 , GRCh38.p12 chr14: 73,534,407-73,563,195	HEATR4, ACOT1, 1 more genes
nsv4381249	copy number variation	16	nstd173	human		GRCh37 chr3: 98,936,926-98,964,849 , GRCh38.p12 chr3: 99,218,082-99,246,005	0
nsv4387023	copy number variation	344	nstd173	human		GRCh37 chr2: 34,701,643-34,727,784 , GRCh38.p12 chr2: 34,476,576-34,502,717	0
nsv4379987	copy number variation	105	nstd173	human		GRCh37 chr14: 86,284,754-86,309,385 , GRCh38.p12 chr14: 85,818,410-85,843,041	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

2-1526-003 AND nstd173 (15)
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)