2-1291-003 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4377883	copy number variation	50	nstd173	human	GRCh37 chr14: 41,610,544-41,657,457 , GRCh38.p12 chr14: 41,141,341-41,188,254	LINC02315
nsv4385917	copy number variation	155	nstd173	human	GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4372198	copy number variation	20	nstd173	human	GRCh37 chr6: 124,435,286-124,470,365 , GRCh38.p12 chr6: 124,114,141-124,149,220	NKAIN2
nsv4366234	copy number variation	14	nstd173	human	GRCh37 chr7: 75,354,113-75,378,713 , GRCh38.p12 chr7: 75,724,795-75,749,395	HIP1
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
nsv4372080	copy number variation	569	nstd173	human	GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4387741	copy number variation	1	nstd173	human	GRCh37 chr7: 26,201,469-26,227,560 , GRCh38.p12 chr7: 26,161,849-26,187,940	NFE2L3, HNRNPA2B1
nsv4378542	copy number variation	1	nstd173	human	GRCh37 chrY: 24,866,936-24,993,248 , GRCh38.p12 chrY: 22,720,789-22,847,101	RBMY2WP, LOC107987348, 1 more genes
nsv4378420	copy number variation	1	nstd173	human	GRCh37 chr9: 28,550,562-28,620,606 , GRCh38.p12 chr9: 28,550,564-28,620,608	LOC105376003, LINGO2, 2 more genes
nsv4387297	copy number variation	1	nstd173	human	GRCh37 chr11: 55,386,384-55,452,560 , GRCh38.p12 chr11: 55,618,908-55,685,084	OR4V1P, OR4P4, 3 more genes
nsv4367001	copy number variation	197	nstd173	human	GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4371991	copy number variation	196	nstd173	human	GRCh37 chr19: 20,596,118-20,720,705 , GRCh38.p12 chr19: 20,413,312-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4384083	copy number variation	1	nstd173	human	GRCh37 chrY: 27,040,718-27,452,092 , GRCh38.p12 chrY: 24,894,571-25,305,945	BPY2C, RBMY2YP, 11 more genes
nsv4379891	copy number variation	2	nstd173	human	GRCh37 chrY: 25,838,208-26,153,100 , GRCh38.p12 chrY: 23,692,061-24,006,953	RAB9AP1, RAB9AP5, 19 more genes
nsv4376368	copy number variation	168	nstd173	human	GRCh37 chr6: 67,009,023-67,048,629 , GRCh38.p12 chr6: 66,299,130-66,338,736	0
nsv4372681	copy number variation	7	nstd173	human	GRCh37 chr12: 31,355,873-31,410,284 , GRCh38.p12 chr12: 31,202,939-31,257,350 , GRCh38.p12 chr12\|NT_187587.1: 93,733-148,144	RPL13AP22, MTND6P26, 4 more genes
nsv4386656	copy number variation	1	nstd173	human	GRCh37 chr14: 107,145,551-107,179,594 , GRCh38.p12 chr14: 106,689,534-106,771,352	IGHV2-70D, IGHVIII-67-3, 8 more genes
nsv4373196	copy number variation	38	nstd173	human	GRCh37 chr6: 29,841,021-29,899,646 , GRCh38.p12 chr6: 29,873,244-29,931,869	DDX39BP1, HCG4P7, 8 more genes
nsv4372589	copy number variation	741	nstd173	human	GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0
nsv4374014	copy number variation	33	nstd173	human	GRCh37 chr5: 57,326,267-57,349,986 , GRCh38.p12 chr5: 58,030,440-58,054,159	0

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: 20

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity