IS38057 AND nstd71 - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 19

loading data ...

Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv904141	copy number variation	3	nstd71	human		NCBI36 chr15: 41,063,637-41,179,367 , GRCh37.p13 chr15: 43,276,345-43,392,075 , GRCh38.p12 chr15: 42,984,147-43,099,877	UBR1
nsv898037	copy number variation	2	nstd71	human		NCBI36 chr11: 84,109,695-84,171,525 , GRCh37.p13 chr11: 84,432,047-84,493,877 , GRCh38.p12 chr11: 84,721,004-84,782,834	DLG2
nsv894410	copy number variation	1	nstd71	human		NCBI36 chr9: 138,606,913-138,638,539 , GRCh37.p13 chr9: 139,487,092-139,518,718 , GRCh38.p12 chr9: 136,592,640-136,624,266	LINC01451
nsv872146	copy number variation	9	nstd71	human		NCBI36 chr1: 111,161,325-111,192,904 , GRCh37.p13 chr1: 111,359,802-111,391,381 , GRCh38.p12 chr1: 110,817,180-110,848,759	NRBF2P3
nsv902185	copy number variation	1	nstd71	human		NCBI36 chr14: 91,484,133-91,529,711 , GRCh37.p13 chr14: 92,414,380-92,459,958 , GRCh38.p12 chr14: 91,948,036-91,993,614	FBLN5, TRIP11
nsv910272	copy number variation	10	nstd71	human		NCBI36 chr19: 677,098-715,389 , GRCh37.p13 chr19: 726,098-764,389 , GRCh38.p12 chr19: 726,098-764,389	MISP, PALM
nsv870557	copy number variation	1	nstd71	human		NCBI36 chr1: 9,240,988-9,323,455 , GRCh37.p13 chr1: 9,318,401-9,400,868 , GRCh38.p12 chr1: 9,258,342-9,340,809	SPSB1, H6PD
nsv904945	copy number variation	9	nstd71	human		NCBI36 chr16: 1,110,513-1,218,038 , GRCh37.p13 chr16: 1,170,512-1,278,037 , GRCh38.p12 chr16: 1,120,512-1,228,037	TPSB2, LOC105371042, 2 more genes
nsv908437	copy number variation	1	nstd71	human		NCBI36 chr17: 41,788,595-41,886,849 , GRCh37.p13 chr17: 44,432,855-44,531,539 , GRCh38.p12 chr17\|NT_187663.1: 1,118,390-1,181,521 , GRCh38.p12 chr17: 46,355,489-46,454,173	NSFP1, ARL17B, 1 more genes
nsv891785	copy number variation	14	nstd71	human		NCBI36 chr8: 145,050,595-145,133,612 , GRCh37.p13 chr8: 144,978,607-145,061,624 , GRCh37.p13 chr8\|NW_003315923.1: 243,084-326,101 , GRCh38.p12 chr8: 143,904,439-143,987,456	PARP10, PLEC, 1 more genes
nsv882084	copy number variation	25	nstd71	human		NCBI36 chr5: 70,232,726-70,300,876 , GRCh37.p13 chr5: 70,196,970-70,265,120 , GRCh38.p12 chr5: 70,901,143-70,969,293	SERF1A, NAIP, 2 more genes
nsv875403	copy number variation	15	nstd71	human		NCBI36 chr2: 170,051,329-170,110,953 , GRCh37.p13 chr2: 170,343,083-170,402,707 , GRCh38.p12 chr2: 169,486,573-169,546,197	FASTKD1, BBS5, 1 more genes
nsv910609	copy number variation	3	nstd71	human		NCBI36 chr19: 1,983,148-2,048,832 , GRCh37.p13 chr19: 2,032,148-2,097,832 , GRCh38.p12 chr19: 2,032,149-2,097,833	MKNK2, LOC107985278, 2 more genes
nsv891829	copy number variation	3	nstd71	human		NCBI36 chr8: 145,434,293-145,529,349 , GRCh37.p13 chr8: 145,463,485-145,558,541 , GRCh37.p13 chr8\|NW_003315924.1: 38,657-104,138 , GRCh38.p12 chr8: 144,268,946-144,334,879	HSF1, BOP1, 4 more genes
nsv910512	copy number variation	2	nstd71	human		NCBI36 chr19: 1,399,180-1,531,334 , GRCh37.p13 chr19: 1,448,180-1,580,334 , GRCh38.p12 chr19: 1,448,181-1,580,335	APC2, PCSK4, 8 more genes
nsv884228	copy number variation	228	nstd71	human		NCBI36 chr6: 31,385,967-31,398,785 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,624,528 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh37.p13 chr6: 31,277,988-31,290,806 , GRCh38.p12 chr6: 31,310,211-31,323,029 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,625,230	0
nsv885750	copy number variation	1	nstd71	human		NCBI36 chr6: 33,064,432-33,075,506 , GRCh37.p13 chr6: 32,956,454-32,967,528 , GRCh37.p13 chr6\|NT_167245.1: 4,237,795-4,248,878 , GRCh38.p12 chr6\|NT_167245.2: 4,232,210-4,243,293 , GRCh38.p12 chr6: 32,988,677-32,999,751	0
nsv884136	copy number variation	3	nstd71	human		NCBI36 chr6: 31,144,762-31,152,501 , GRCh37.p13 chr6: 31,036,783-31,044,522 , GRCh37.p13 chr6\|NT_167247.1: 2,418,707-2,426,446 , GRCh37.p13 chr6\|NT_167246.1: 2,385,133-2,392,868 , GRCh38.p12 chr6\|NT_167247.2: 2,413,122-2,420,861 , GRCh38.p12 chr6\|NT_167246.2: 2,379,513-2,387,248 , GRCh38.p12 chr6: 31,069,006-31,076,745	0
nsv875055	copy number variation	2	nstd71	human		NCBI36 chr2: 130,508,683-130,901,823 , GRCh37.p13 chr2: 130,792,213-131,185,353 , GRCh38.p12 chr2: 130,034,640-130,427,780	CCDC74B, TRE-TTC1-1, 33 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

IS38057 AND nstd71 (20)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)