16-1020-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4366402	copy number variation	12	nstd173	human		GRCh37 chr4: 34,779,032-34,831,805 , GRCh38.p12 chr4: 34,777,410-34,830,183 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-322,512	LOC105378262
nsv4381717	copy number variation	19	nstd173	human		GRCh37 chr16: 55,796,376-55,816,692 , GRCh38.p12 chr16: 55,762,464-55,782,780	CES1P1
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
nsv4381602	copy number variation	1	nstd173	human		GRCh37 chr3: 32,037,301-32,071,038 , GRCh38.p12 chr3: 31,995,809-32,029,546	RPL21P40, ZNF860
nsv4376403	copy number variation	119	nstd173	human		GRCh37 chr19: 53,517,242-53,553,087 , GRCh38.p12 chr19: 53,013,989-53,049,834	ERVV-1, ERVV-2
nsv4386054	copy number variation	20	nstd173	human		GRCh37 chr11: 55,374,176-55,442,305 , GRCh38.p12 chr11: 55,606,700-55,674,829	OR4S2, OR4C6, 2 more genes
nsv4368241	copy number variation	217	nstd173	human		GRCh37 chr17: 34,437,482-34,477,480 , GRCh38.p12 chr17: 36,110,089-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,186-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,010-385,008	LOC100419980, LOC101927369, 3 more genes
nsv4369919	copy number variation	116	nstd173	human		GRCh37 chr14: 106,530,472-106,667,035 , GRCh38.p12 chr14: 106,074,229-106,210,392 , GRCh38.p12 chr14\|NT_187600.1: 541,998-678,161	IGHV1-18, IGHV3-20, 17 more genes
nsv4378809	copy number variation	20	nstd173	human		GRCh37 chr5: 140,218,726-140,253,787 , GRCh38.p12 chr5: 140,839,141-140,874,202	PCDHA7, PCDHA4, 13 more genes
nsv4374133	copy number variation	39	nstd173	human		GRCh37 chr3: 175,883,703-175,916,315 , GRCh38.p12 chr3: 176,165,915-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 50,426-83,038	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
nsv4368210	copy number variation	12	nstd173	human		GRCh37 chr8: 34,832,362-34,854,498 , GRCh38.p12 chr8: 34,974,844-34,996,980	0
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4378472	copy number variation	11	nstd173	human		GRCh37 chr10: 46,966,534-48,203,688 , GRCh38.p12 chr10: 46,157,935-47,923,579	AGAP13P, FAM25BP, 54 more genes
nsv4368196	copy number variation	1	nstd173	human		GRCh37 chr14: 22,563,614-22,960,757 , GRCh38.p12 chr14: 22,095,337-22,491,770	TRAV33, TRAJ60, 52 more genes
nsv4388479	copy number variation	8	nstd173	human		GRCh37 chr7: 38,319,296-38,382,540 , GRCh38.p12 chr7: 38,279,695-38,342,939	TRGV7, TRG-AS1, 10 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
nsv4387382	copy number variation	84	nstd173	human		GRCh37 chr5: 57,326,026-57,349,970 , GRCh38.p12 chr5: 58,030,199-58,054,143	0

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