MS19698 AND nstd71 - dbVar - NCBI

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

Search results

Items: 14

loading data ...

Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv884822	copy number variation	2547	nstd71	human		NCBI36 chr6: 32,560,168-32,593,470 , GRCh37.p13 chr6: 32,452,190-32,485,492 , GRCh38.p12 chr6: 32,484,413-32,517,715	HLA-DRB5
nsv908380	copy number variation	142	nstd71	human		NCBI36 chr17: 41,775,690-41,943,845 , GRCh37.p13 chr17: 44,419,932-44,588,529 , GRCh38.p12 chr17: 46,342,566-46,511,163	LRRC37A2, ARL17A, 3 more genes
nsv904062	copy number variation	7	nstd71	human		NCBI36 chr15: 32,530,131-32,625,184 , GRCh37.p13 chr15: 34,742,839-34,837,892 , GRCh38.p12 chr15: 34,450,638-34,545,691	FSCN1P1, DNM1P5, 3 more genes
nsv883738	copy number variation	13	nstd71	human		NCBI36 chr6: 29,972,294-29,986,717 , GRCh37.p13 chr6\|NT_167246.1: 1,158,492-1,172,914 , GRCh37.p13 chr6: 29,864,315-29,878,738 , GRCh38.p12 chr6: 29,896,538-29,910,961 , GRCh38.p12 chr6\|NT_167246.2: 1,152,872-1,167,294	HLA-A, DDX39BP1, 3 more genes
nsv879604	copy number variation	1	nstd71	human		NCBI36 chr4: 93,283,210-93,506,767 , GRCh37.p13 chr4: 93,064,187-93,287,744 , GRCh38.p12 chr4: 92,143,036-92,366,593	LNCPRESS2, PMPCAP1, 1 more genes
nsv902761	copy number variation	101	nstd71	human		NCBI36 chr15: 19,031,743-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,729,748-21,258,351	POTEB2, MIR5701-1, 22 more genes
nsv887001	copy number variation	155	nstd71	human		NCBI36 chr6: 169,246,516-169,271,889 , GRCh37.p13 chr6: 169,504,591-169,529,964 , GRCh38.p12 chr6: 169,104,496-169,129,869	0
nsv884226	copy number variation	67	nstd71	human		NCBI36 chr6: 31,385,967-31,396,472 , GRCh37.p13 chr6: 31,277,988-31,288,493 , GRCh37.p13 chr6\|NT_167249.1: 2,611,726-2,622,207 , GRCh37.p13 chr6\|NT_167246.1: 2,624,814-2,631,393 , GRCh38.p12 chr6\|NT_167246.2: 2,619,194-2,625,775 , GRCh38.p12 chr6\|NT_167249.2: 2,612,428-2,622,909 , GRCh38.p12 chr6: 31,310,211-31,320,716	0
nsv906451	copy number variation	1	nstd71	human		NCBI36 chr16: 32,472,584-32,481,352 , GRCh37.p13 chr16: 32,565,083-32,573,851 , GRCh38.p12 chr16: 32,553,762-32,562,530	0
nsv896769	copy number variation	1	nstd71	human		NCBI36 chr11: 1,958,471-2,052,309 , GRCh37.p13 chr11: 2,001,895-2,095,733 , GRCh38.p12 chr11: 1,980,665-2,074,503	LINC01219, MRPL23, 3 more genes
nsv903247	copy number variation	118	nstd71	human		NCBI36 chr15: 19,635,853-20,203,694 , GRCh37.p13 chr15: 21,371,194-22,652,330 , GRCh38.p12 chr15: 21,165,865-22,308,242	OR11J6P, LOC642131, 56 more genes
nsv903078	copy number variation	34	nstd71	human		NCBI36 chr15: 19,341,464-19,556,128 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,924,655-21,498,353	OR11J2P, LOC105370715, 23 more genes
nsv896728	copy number variation	1	nstd71	human		NCBI36 chr11: 1,639,330-1,884,793 , GRCh37.p13 chr11: 1,682,754-1,928,217 , GRCh38.p12 chr11: 1,661,524-1,906,987	TNNI2, FAM99A, 14 more genes
nsv888197	copy number variation	1	nstd71	human		NCBI36 chr7: 61,667,556-61,813,750 , GRCh37.p13 chr7: 62,030,121-62,176,315 , GRCh38.p12 chr7: 62,569,743-62,715,937	0

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

MS19698 AND nstd71 (15)
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)