MS19023 AND nstd71 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv874997	copy number variation	8	nstd71	human		NCBI36 chr2: 126,519,270-126,773,004 , GRCh37.p13 chr2: 126,802,800-127,056,534 , GRCh38.p12 chr2: 126,045,223-126,298,957	LINC01941
nsv876855	copy number variation	1	nstd71	human		NCBI36 chr3: 60,423,301-60,475,589 , GRCh37.p13 chr3: 60,448,261-60,500,549 , GRCh38.p12 chr3: 60,462,528-60,514,816	FHIT
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
nsv874909	copy number variation	74	nstd71	human		NCBI36 chr2: 115,231,523-115,253,261 , GRCh37.p13 chr2: 115,515,053-115,536,791 , GRCh38.p12 chr2: 114,757,476-114,779,214	DPP10
nsv909839	copy number variation	966	nstd71	human		NCBI36 chr18: 64,895,268-64,909,808 , GRCh37.p13 chr18: 66,744,288-66,758,828 , GRCh38.p12 chr18: 69,077,051-69,091,591	CCDC102B
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv906363	copy number variation	2	nstd71	human		NCBI36 chr16: 32,465,671-32,579,320 , GRCh37.p13 chr16: 32,558,170-32,671,819 , GRCh38.p12 chr16: 32,546,849-32,660,498	LOC107984013, FAM153DP
nsv893264	copy number variation	10	nstd71	human		NCBI36 chr9: 43,609,749-43,720,352 , GRCh37.p13 chr9: 43,669,753-43,780,356 , GRCh38.p12 chr9: 42,034,033-42,144,636	CNTNAP3B, LOC100420440
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv889331	copy number variation	5	nstd71	human		NCBI36 chr7: 143,100,579-143,167,358 , GRCh37.p13 chr7: 143,469,646-143,536,425 , GRCh38.p12 chr7: 143,772,553-143,839,332 , GRCh38.p12 chr7\|NW_018654714.1: 316,876-383,635	TCAF2P1, LOC154761, 3 more genes
nsv905933	copy number variation	3	nstd71	human		NCBI36 chr16: 32,406,646-32,429,465 , GRCh37.p13 chr16: 32,499,145-32,521,964 , GRCh38.p12 chr16: 32,487,824-32,510,643	0
nsv874830	copy number variation	2	nstd71	human		NCBI36 chr2: 110,258,184-111,021,091 , GRCh37.p13 chr2: 110,900,895-111,334,482 , GRCh38.p12 chr2: 110,143,318-110,576,877	MIR4436B2, LINC01106, 15 more genes
nsv895206	copy number variation	1	nstd71	human		NCBI36 chr10: 46,801,296-47,171,576 , GRCh37.p13 chr10: 47,381,290-47,689,665 , GRCh38.p12 chr: NaN-NaN	0
nsv901351	copy number variation	15	nstd71	human		NCBI36 chr14: 19,288,965-19,494,891 , GRCh37.p13 chr14: 20,219,125-20,425,051 , GRCh38.p12 chr14: 19,750,966-19,956,892	OR4K6P, OR4K16P, 11 more genes

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MS19023 AND nstd71 (15)
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