14-0276-001 AND nstd173 - dbVar - NCBI

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Items: 18

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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
nsv4372152	copy number variation	236	nstd173	human		GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467	LOC105377865
nsv4367263	copy number variation	26	nstd173	human		GRCh37 chr4: 34,779,032-34,831,780 , GRCh38.p12 chr4: 34,777,410-34,830,158 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-322,487	LOC105378262
nsv4368058	copy number variation	90	nstd173	human		GRCh37 chr5: 97,043,561-97,093,733 , GRCh38.p12 chr5: 97,707,857-97,758,029	LOC391813
nsv4387987	copy number variation	22	nstd173	human		GRCh37 chr11: 49,710,692-49,758,260 , GRCh38.p12 chr11: 49,689,140-49,736,708 , GRCh38.p12 chr11\|NW_019805495.1: 153,322-200,857	GRM5P1
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
nsv4377726	copy number variation	23	nstd173	human		GRCh37 chr6: 55,823,233-55,843,659 , GRCh38.p12 chr6: 55,958,435-55,978,861	LOC107986539
nsv4386329	copy number variation	1	nstd173	human		GRCh37 chr9: 110,210,658-110,233,097 , GRCh38.p12 chr9: 107,448,377-107,470,816	LINC01509, HMGN2P32
nsv4383034	copy number variation	5	nstd173	human		GRCh37 chr8: 39,246,760-39,389,003 , GRCh38.p12 chr8: 39,389,241-39,531,484	ADAM5, ADAM3A
nsv4382253	copy number variation	206	nstd173	human		GRCh37 chr12: 11,503,225-11,553,849 , GRCh38.p12 chr12: 11,350,291-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,254-572,349	PRB2, PRB1
nsv4367864	copy number variation	2	nstd173	human		GRCh37 chr19: 55,307,868-55,333,826 , GRCh38.p12 chr19\|NT_187693.1: 778,982-804,940	KIR2DL4, KIR3DL1
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4378165	copy number variation	86	nstd173	human		GRCh37 chr4: 69,435,889-69,540,420 , GRCh38.p12 chr4: 68,570,171-68,674,702	UGT2B17, LOC100422402, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 3 more genes
nsv4374249	copy number variation	1	nstd173	human		GRCh37 chr14: 106,072,251-106,716,559 , GRCh38.p12 chr14: 105,786,368-106,259,962 , GRCh38.p12 chr14\|NT_187600.1: 73,683-1,214,078	IGHD1-14, IGHVIII-13-1, 182 more genes
nsv4365131	copy number variation	54	nstd173	human		GRCh37 chr14: 22,404,167-22,974,280 , GRCh38.p12 chr14: 21,935,993-22,505,293	TRAJ46, TRAJ57, 76 more genes
nsv4380176	copy number variation	3	nstd173	human		GRCh37 chr7: 142,227,556-142,475,287 , GRCh38.p12 chr7\|NT_187562.1: 622,348-792,624	TRBV26, PRSS1, 19 more genes
nsv4367766	copy number variation	3	nstd173	human		GRCh37 chr7: 38,319,296-38,395,208 , GRCh38.p12 chr7: 38,279,695-38,355,607	TRGV4, TRGV6, 13 more genes

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