5-0034-003 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4382434	copy number variation	1	nstd173	human	GRCh37 chr10: 68,281,037-68,415,535 , GRCh38.p12 chr10: 66,521,279-66,655,777	CTNNA3
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
nsv4375716	copy number variation	91	nstd173	human	GRCh37 chr3: 165,041,535-165,085,386 , GRCh38.p12 chr3: 165,323,747-165,367,598	LINC01322
nsv4371909	copy number variation	1	nstd173	human	GRCh37 chr10: 61,486,937-61,528,516 , GRCh38.p12 chr10: 59,727,179-59,768,758	MRLN
nsv4379109	copy number variation	1337	nstd173	human	GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4384091	copy number variation	77	nstd173	human	GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4381127	copy number variation	1	nstd173	human	GRCh37 chr8: 53,650,054-53,754,959 , GRCh38.p12 chr8: 52,737,494-52,842,399	LOC105375835
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
nsv4377379	copy number variation	45	nstd173	human	GRCh37 chr3: 46,793,072-46,849,576 , GRCh38.p12 chr3: 46,751,582-46,808,086	PRSS43P, PRSS44P
nsv4383863	copy number variation	1	nstd173	human	GRCh37 chr12: 51,364,259-51,400,825 , GRCh38.p12 chr12: 50,970,476-51,007,042	SLC11A2, HIGD1C
nsv4380294	copy number variation	1	nstd173	human	GRCh37 chr5: 17,491,269-17,513,409 , GRCh38.p12 chr5: 17,491,160-17,513,300	H3Y2, H3P18, 1 more genes
nsv4369049	copy number variation	64	nstd173	human	GRCh37 chr12: 8,004,412-8,124,048 , GRCh38.p12 chr12: 7,851,816-7,971,452	NANOGP1, SLC2A14, 3 more genes
nsv4370277	copy number variation	687	nstd173	human	GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 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
nsv4376250	copy number variation	1	nstd173	human	GRCh37 chr11: 55,685,799-55,823,617 , GRCh38.p12 chr11: 55,918,323-56,056,141	OR5I1, OR5F2P, 7 more genes
nsv4386776	copy number variation	36	nstd173	human	GRCh37 chr2: 78,701,691-78,727,518 , GRCh38.p12 chr2: 78,474,565-78,500,392	0
nsv4374553	copy number variation	6	nstd173	human	GRCh37 chr12: 21,567,402-21,588,168 , GRCh38.p12 chr12: 21,414,468-21,435,234	0
nsv4385677	copy number variation	32	nstd173	human	GRCh37 chr19: 54,722,728-54,752,217 , GRCh38.p12 chr19: 54,218,859-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 193,842-223,331 , GRCh38.p12 chr19\|NW_003571061.2: 193,842-223,362 , GRCh38.p12 chr19\|NW_003571060.1: 193,845-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 193,659-223,093	LOC102725035, LILRB5, 7 more genes
nsv4373457	copy number variation	3	nstd173	human	GRCh37 chr8: 42,935,730-43,824,035 , GRCh38.p12 chr8: 43,080,587-43,968,892	VN1R46P, SNX18P27, 13 more genes
nsv4381676	copy number variation	1	nstd173	human	GRCh37 chr2: 98,017,804-98,162,176 , GRCh38.p12 chr: NaN-NaN	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