2-1736-003 AND nstd173 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv4386779	copy number variation	33	nstd173	human	GRCh37 chr7: 141,755,372-141,799,117 , GRCh38.p12 chr7: 142,055,572-142,099,317 , GRCh38.p12 chr7\|NT_187562.1: 17,452-61,197	MGAM
nsv4369241	copy number variation	1	nstd173	human	GRCh37 chr12: 43,412,455-43,450,536 , GRCh38.p12 chr12: 43,018,652-43,056,733	MRPS36P5
nsv4371742	copy number variation	24	nstd173	human	GRCh37 chr11: 4,970,265-4,991,060 , GRCh38.p12 chr11: 4,949,035-4,969,830	OR51A2
nsv4385871	copy number variation	3	nstd173	human	GRCh37 chr14: 86,460,915-86,500,283 , GRCh38.p12 chr14: 85,994,571-86,033,939	LINC02328, LINC02316
nsv4386355	copy number variation	1	nstd173	human	GRCh37 chr7: 127,487,780-127,520,547 , GRCh38.p12 chr7: 127,847,727-127,880,494	LOC100196944, SND1
nsv4381915	copy number variation	18	nstd173	human	GRCh37 chr8: 39,246,772-39,386,952 , GRCh38.p12 chr8: 39,389,253-39,529,433	ADAM3A, ADAM5
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
nsv4380407	copy number variation	3	nstd173	human	GRCh37 chr11: 55,373,995-55,442,305 , GRCh38.p12 chr11: 55,606,519-55,674,829	OR4V1P, OR4S2, 2 more genes
nsv4381284	copy number variation	16	nstd173	human	GRCh37 chr4: 69,435,901-69,484,109 , GRCh38.p12 chr4: 68,570,183-68,618,391	LOC100422402, UGT2B17, 1 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
nsv4386828	copy number variation	67	nstd173	human	GRCh37 chr19: 20,596,118-20,716,388 , GRCh38.p12 chr19: 20,413,312-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4385929	copy number variation	5	nstd173	human	GRCh37 chr17: 36,243,051-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 2,122,116-2,289,624	LOC102723851, NPEPPSP1, 8 more genes
nsv4379762	copy number variation	26	nstd173	human	GRCh37 chr6: 29,864,521-29,936,041 , GRCh38.p12 chr6: 29,896,744-29,968,264	HCG4B, HCG4P4, 9 more genes
nsv4375266	copy number variation	23	nstd173	human	GRCh37 chr2: 4,208,245-4,242,370 , GRCh38.p12 chr2: 4,160,655-4,194,780	0
nsv4388075	copy number variation	1	nstd173	human	GRCh37 chr3: 98,936,926-98,969,676 , GRCh38.p12 chr3: 99,218,082-99,250,832	0
nsv4369957	copy number variation	137	nstd173	human	GRCh37 chr10: 46,966,546-47,149,423 , GRCh38.p12 chr10: 46,400,340-46,583,071	GPRIN2, , 5 more genes
nsv4385506	copy number variation	1	nstd173	human	GRCh37 chr14: 107,153,192-107,179,594 , GRCh38.p12 chr14: 106,697,175-106,771,352	IGHV1-68, IGHV2-70, 6 more genes
nsv4365103	copy number variation	2	nstd173	human	GRCh37 chr12: 31,356,049-31,407,110 , GRCh38.p12 chr12: 31,203,115-31,254,176 , GRCh38.p12 chr12\|NT_187587.1: 93,909-144,970	RPL13AP22, MTND6P26, 4 more genes
nsv4379744	copy number variation	1	nstd173	human	GRCh37 chr14: 22,663,655-22,893,999 , GRCh38.p12 chr14: 22,195,761-22,425,008	TRAV35, TRD, 14 more genes
nsv4371769	copy number variation	51	nstd173	human	GRCh37 chr11: 54,701,632-54,762,018 , GRCh38.p12 chr11: 54,934,156-54,994,542	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