212972 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4369684	copy number variation	1	nstd173	human	GRCh37 chr2: 52,827,580-52,893,232 , GRCh38.p12 chr2: 52,600,442-52,666,094	FTH1P6
nsv4380190	copy number variation	32	nstd173	human	GRCh37 chr2: 98,079,569-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713	ANKRD36B
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
nsv4382001	copy number variation	14	nstd173	human	GRCh37 chr13: 69,242,149-69,268,719 , GRCh38.p12 chr13: 68,668,017-68,694,587	RN7SL761P
nsv4386644	copy number variation	2	nstd173	human	GRCh37 chr3: 128,377,071-128,399,208 , GRCh38.p12 chr3: 128,658,228-128,680,365	POU5F1P6
nsv4384033	copy number variation	5	nstd173	human	GRCh37 chr4: 58,053,877-58,100,454 , GRCh38.p12 chr4: 57,187,711-57,234,288	IGFBP7-AS1
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
nsv4383929	copy number variation	6	nstd173	human	GRCh37 chr14: 86,460,977-86,487,665 , GRCh38.p12 chr14: 85,994,633-86,021,321	LINC02328, LINC02316
nsv4383109	copy number variation	49	nstd173	human	GRCh37 chr11: 55,374,031-55,453,575 , GRCh38.p12 chr11: 55,606,555-55,686,099	OR4P1P, OR4P4, 3 more genes
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
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
nsv4386129	copy number variation	134	nstd173	human	GRCh37 chr17: 34,439,977-34,477,480 , GRCh38.p12 chr17: 36,112,584-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,681-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,505-385,008	LOC101927369, LOC100419980, 2 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
nsv4370840	copy number variation	154	nstd173	human	GRCh37 chr12: 11,222,368-11,247,388 , GRCh38.p12 chr12: 11,069,769-11,094,789	TAS2R43, TAS2R64P, 3 more genes
nsv4378128	copy number variation	463	nstd173	human	GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4376583	copy number variation	23	nstd173	human	GRCh37 chr6: 31,280,867-31,314,589 , GRCh38.p12 chr6: 31,313,090-31,346,812	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
nsv4375938	copy number variation	4	nstd173	human	GRCh37 chr14: 22,635,680-22,959,555 , GRCh38.p12 chr14: 22,167,784-22,490,567	TRDJ2, TRAJ57, 42 more genes
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