5-0106-001 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4383050	copy number variation	1	nstd173	human	GRCh37 chr18: 1,724,055-1,838,179 , GRCh38.p12 chr18: 1,724,054-1,838,178 , GRCh38.p12 chr18\|NW_019805503.1: 1-93,974	LOC105371959
nsv4371805	copy number variation	282	nstd173	human	GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4372379	copy number variation	1	nstd173	human	GRCh37 chr4: 172,259,271-172,529,147 , GRCh38.p12 chr4: 171,338,120-171,607,996	LINC02174, LOC105377535
nsv4378013	copy number variation	3	nstd173	human	GRCh37 chr17: 21,345,001-21,510,992 , GRCh38.p12 chr17: 21,441,689-21,607,725	LINC02693, LOC100533653, 3 more genes
nsv4384620	copy number variation	51	nstd173	human	GRCh37 chr6: 257,049-294,826 , GRCh38.p12 chr6: 257,049-294,826	DUSP22, , 1 more genes
nsv4367271	copy number variation	561	nstd173	human	GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 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
nsv4375922	copy number variation	10	nstd173	human	GRCh37 chrX: 103,261,175-103,305,297 , GRCh38.p12 chrX: 104,006,603-104,050,731	H2BW2, LOC107985662, 1 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
nsv4369207	copy number variation	1	nstd173	human	GRCh37 chr3: 5,390,506-6,216,818 , GRCh38.p12 chr3: 5,348,821-6,175,131	MRPS35P1, LOC102723596, 6 more genes
nsv4376766	copy number variation	8	nstd173	human	GRCh37 chr16: 32,570,986-32,851,881 , GRCh38.p12 chr16: 32,559,665-32,840,560	TP53TG3, HERC2P5, 6 more genes
nsv4378481	copy number variation	186	nstd173	human	GRCh37 chr2: 4,208,245-4,234,699 , GRCh38.p12 chr2: 4,160,655-4,187,109	0
nsv4382392	copy number variation	421	nstd173	human	GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4371406	copy number variation	8	nstd173	human	GRCh37 chr6: 110,394,605-110,415,232 , GRCh38.p12 chr6: 110,073,402-110,094,029	0
nsv4376676	copy number variation	22	nstd173	human	GRCh37 chrX: 103,171,609-103,236,332 , GRCh38.p12 chrX: 103,917,015-103,981,754	SLC25A53P1, H2BW4P, 4 more genes
nsv4367231	copy number variation	1	nstd173	human	GRCh37 chr1: 242,959,776-243,667,814 , GRCh38.p12 chr1: 242,796,474-243,504,512 , GRCh38.p12 chr1\|NT_187519.1: 1-516,620	, LOC105373249, 12 more genes
nsv4385122	copy number variation	1	nstd173	human	GRCh37 chr14: 22,628,314-22,943,573 , GRCh38.p12 chr14: 22,160,380-22,474,583	TRDV3, TRAV32, 32 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
nsv4374272	copy number variation	58	nstd173	human	GRCh37 chr11: 54,701,632-54,794,727 , GRCh38.p12 chr11: 54,934,156-55,027,251	0
nsv4368473	copy number variation	289	nstd173	human	GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	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