2-1408-001 AND nstd173 - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4367737	copy number variation	1	nstd173	human		GRCh37 chr6: 141,957,504-142,086,922 , GRCh38.p12 chr6: 141,636,367-141,765,785	RPS3AP23
nsv4375206	copy number variation	7	nstd173	human		GRCh37 chrX: 2,281,872-2,303,322 , GRCh38.p12 chrX: 2,363,831-2,385,281	DHRSX
nsv4371574	copy number variation	3	nstd173	human		GRCh37 chr6: 254,254-381,148 , GRCh38.p12 chr6: 254,254-381,148	, , 1 more genes
nsv4369825	copy number variation	122	nstd173	human		GRCh37 chr4: 69,435,901-69,540,429 , GRCh38.p12 chr4: 68,570,183-68,674,711	UGT2B15, LOC100422402, 3 more genes
nsv4386376	copy number variation	1	nstd173	human		GRCh37 chr16: 32,848,683-32,902,151 , GRCh38.p12 chr16: 32,837,362-32,890,830	IGHV2OR16-5, BCAP31P2, 1 more genes
nsv4381549	copy number variation	39	nstd173	human		GRCh37 chr20: 44,348,549-44,381,615 , GRCh38.p12 chr20: 45,719,910-45,752,976	HNRNPA1P3, WFDC3, 2 more genes
nsv4365715	copy number variation	8	nstd173	human		GRCh37 chr11: 55,374,176-55,435,179 , GRCh38.p12 chr11: 55,606,700-55,667,703	OR4P4, OR4S2, 1 more genes
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 more genes
nsv4370846	copy number variation	105	nstd173	human		GRCh37 chr12: 11,216,817-11,251,861 , GRCh38.p12 chr12: 11,064,218-11,099,262	PRH1, PRH1-PRR4, 3 more genes
nsv4382124	copy number variation	1	nstd173	human		GRCh37 chr16: 32,937,323-33,779,366 , GRCh38.p12 chr16: 32,926,002-33,976,899	IGHV3OR16-8, ABHD17AP9, 31 more genes
nsv4385955	copy number variation	154	nstd173	human		GRCh37 chr3: 162,521,309-162,626,676 , GRCh38.p12 chr3: 162,803,521-162,908,888	0
nsv4374875	copy number variation	271	nstd173	human		GRCh37 chr6: 67,009,023-67,051,189 , GRCh38.p12 chr6: 66,299,130-66,341,296	0
nsv4386560	copy number variation	16	nstd173	human		GRCh37 chr14: 86,284,754-86,316,105 , GRCh38.p12 chr14: 85,818,410-85,849,761	0
nsv4378032	copy number variation	1	nstd173	human		GRCh37 chr12: 74,377,998-74,409,134 , GRCh38.p12 chr12: 73,984,218-74,015,354	0
nsv4374783	copy number variation	2	nstd173	human		GRCh37 chr4: 104,737,967-104,763,949 , GRCh38.p12 chr4: 103,816,810-103,842,792	0
nsv4372619	copy number variation	1	nstd173	human		GRCh37 chr2: 695,785-922,555 , GRCh38.p12 chr2: 695,785-926,869 , GRCh38.p12 chr2\|NT_187525.1: 1-136,240	LINC01939, , 4 more genes
nsv4384195	copy number variation	3	nstd173	human		GRCh37 chr14: 106,525,222-106,849,677 , GRCh38.p12 chr14: 106,068,977-106,393,766 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGHVII-51-2, IGHVII-30-1, 113 more genes
nsv4387080	copy number variation	1	nstd173	human		GRCh37 chr14: 22,643,684-22,941,066 , GRCh38.p12 chr14: 22,175,787-22,472,076	TRDD3, TRDC, 27 more genes

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