14-0170-004 AND nstd173 - dbVar - NCBI

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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
nsv4369656	copy number variation	16	nstd173	human		GRCh37 chr5: 9,901,952-9,926,287 , GRCh38.p12 chr5: 9,901,840-9,926,175	LINC02112
nsv4365341	copy number variation	37	nstd173	human		GRCh37 chr14: 24,445,622-24,479,697 , GRCh38.p12 chr14: 23,976,413-24,010,488 , GRCh38.p12 chr14\|NW_018654722.1: 273,828-316,310	DHRS4L2, DHRS4L1
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
nsv4373665	copy number variation	1	nstd173	human		GRCh37 chr14: 100,898,748-100,972,431 , GRCh38.p12 chr14: 100,432,411-100,506,094	WDR25, HMGN1P25, 1 more genes
nsv4372238	copy number variation	1	nstd173	human		GRCh37 chr7: 47,723,549-47,945,846 , GRCh38.p12 chr7: 47,683,951-47,906,249	PKD1L1-AS1, LINC00525, 1 more genes
nsv4366220	copy number variation	1	nstd173	human		GRCh37 chr5: 175,592,754-175,751,408 , GRCh38.p12 chr5: 176,165,751-176,324,405	SIMC1, LOC107986487, 2 more genes
nsv4380527	copy number variation	4	nstd173	human		GRCh37 chr17: 44,187,492-44,292,742 , GRCh38.p12 chr17: 46,110,126-46,215,376 , GRCh38.p12 chr17\|NT_187663.1: 812,225-917,549	LOC107985027, KANSL1, 1 more genes
nsv4366696	copy number variation	4	nstd173	human		GRCh37 chr11: 55,374,019-55,462,994 , GRCh38.p12 chr11: 55,606,543-55,695,518	OR4C6, OR4S2, 3 more genes
nsv4378824	copy number variation	33	nstd173	human		GRCh37 chr14: 74,001,111-74,038,551 , GRCh38.p12 chr14: 73,534,407-73,571,847	HEATR4, ACOT1, 3 more genes
nsv4385606	copy number variation	9	nstd173	human		GRCh37 chr6: 257,340-294,431 , GRCh38.p12 chr6: 257,340-294,431	, DUSP22, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4383920	copy number variation	1	nstd173	human		GRCh37 chr8: 12,752,616-12,786,729 , GRCh38.p12 chr8: 12,895,107-12,929,220 , GRCh38.p12 chr8\|NW_018654717.1: 6,090,475-6,124,613	0
nsv4377206	copy number variation	4	nstd173	human		GRCh37 chr14: 86,284,754-86,318,113 , GRCh38.p12 chr14: 85,818,410-85,851,769	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
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4374331	copy number variation	8	nstd173	human		GRCh37 chr2: 4,213,587-4,234,699 , GRCh38.p12 chr2: 4,165,997-4,187,109	0
nsv4381769	copy number variation	2	nstd173	human		GRCh37 chrX: 15,208,755-15,863,090 , GRCh38.p12 chrX: 15,190,633-15,844,967	ACE2, CA5BP1, 17 more genes
nsv4376540	copy number variation	1	nstd173	human		GRCh37 chr14: 22,510,089-22,971,360 , GRCh38.p12 chr14: 22,041,843-22,502,376	TRAV26-1, TRAJ52, 64 more genes
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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