14-0130-002 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
nsv4370579	copy number variation	5	nstd173	human		GRCh37 chr8: 15,944,307-16,024,144 , GRCh38.p12 chr8: 16,086,798-16,166,635	MSR1
nsv4382965	copy number variation	21	nstd173	human		GRCh37 chr2: 98,063,371-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713	ANKRD36B
nsv4386838	copy number variation	2	nstd173	human		GRCh37 chr10: 124,341,428-124,382,030 , GRCh38.p12 chr10: 122,581,912-122,622,514	DMBT1
nsv4375488	copy number variation	51	nstd173	human		GRCh37 chr1: 196,714,810-196,741,354 , GRCh38.p12 chr1: 196,745,680-196,772,224	CFH
nsv4371336	copy number variation	16	nstd173	human		GRCh37 chr11: 4,970,242-4,991,060 , GRCh38.p12 chr11: 4,949,012-4,969,830	OR51A2
nsv4380065	copy number variation	21	nstd173	human		GRCh37 chr1: 72,771,366-72,811,147 , GRCh38.p12 chr1: 72,305,683-72,345,464 , GRCh38.p12 chr1\|NW_018654707.1: 17,950-66,689	LOC105378797
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4376724	copy number variation	112	nstd173	human		GRCh37 chr8: 39,246,772-39,397,015 , GRCh38.p12 chr8: 39,389,253-39,539,496	ADAM5, ADAM3A
nsv4375232	copy number variation	423	nstd173	human		GRCh37 chr5: 180,375,302-180,430,801 , GRCh38.p12 chr5: 180,948,302-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 more genes
nsv4381619	copy number variation	8	nstd173	human		GRCh37 chr12: 11,217,137-11,247,388 , GRCh38.p12 chr12: 11,064,538-11,094,789	TAS2R64P, TAS2R43, 3 more genes
nsv4367942	copy number variation	4	nstd173	human		GRCh37 chr8: 78,614,034-78,762,938 , GRCh38.p12 chr8: 77,701,798-77,850,703	0
nsv4367962	copy number variation	1	nstd173	human		GRCh37 chr9: 11,913,017-12,015,741 , GRCh38.p12 chr9: 11,913,017-12,015,741	0
nsv4365711	copy number variation	3	nstd173	human		GRCh37 chr6: 40,062,884-40,102,313 , GRCh38.p12 chr6: 40,095,145-40,134,574	0
nsv4384699	copy number variation	1	nstd173	human		GRCh37 chr14: 22,548,140-22,966,418 , GRCh38.p12 chr14: 22,079,879-22,497,433	TRA, TRAV38-1, 58 more genes
nsv4388179	copy number variation	3	nstd173	human		GRCh37 chr22: 22,311,349-22,573,197 , GRCh38.p12 chr22: 21,956,977-22,218,805	IGLVI-56, IGLVV-58, 26 more genes
nsv4380112	copy number variation	9	nstd173	human		GRCh37 chr7: 38,319,296-38,400,944 , GRCh38.p12 chr7: 38,279,695-38,361,343	TRGV5, TRGV7, 15 more genes
nsv4368640	copy number variation	11	nstd173	human		GRCh37 chr7: 43,361-65,531 , GRCh38.p12 chr7: 43,361-65,531 , GRCh38.p12 chr7\|NT_187558.1: 1-21,630 , GRCh38.p12 chr7\|NT_187653.1: 35,682-57,852	0

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