4-0001-005 AND nstd173 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4366209	copy number variation	1	nstd173	human		GRCh37 chr1: 190,944,423-191,123,245 , GRCh38.p12 chr1: 190,975,293-191,154,115	HNRNPA1P46
nsv4374794	copy number variation	2	nstd173	human		GRCh37 chr10: 124,319,801-124,382,030 , GRCh38.p12 chr10: 122,560,285-122,622,514	DMBT1
nsv4385079	copy number variation	34	nstd173	human		GRCh37 chr2: 98,141,300-98,162,176 , GRCh38.p12 chr2: 97,524,837-97,545,713	ANKRD36B
nsv4365585	copy number variation	1	nstd173	human		GRCh37 chr7: 98,758,968-98,807,839 , GRCh38.p12 chr7: 99,161,345-99,210,216 , GRCh38.p12 chr7\|NW_017852929.1: 68,974-117,845	KPNA7
nsv4386116	copy number variation	2	nstd173	human		GRCh37 chr9: 72,091,255-72,127,263 , GRCh38.p12 chr9: 69,476,339-69,512,347	APBA1
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
nsv4370203	copy number variation	26	nstd173	human		GRCh37 chr16: 15,049,969-15,126,890 , GRCh38.p12 chr16: 14,956,112-15,033,033	LOC728138, PDXDC1, 1 more genes
nsv4367386	copy number variation	50	nstd173	human		GRCh37 chr6: 257,061-294,826 , GRCh38.p12 chr6: 257,061-294,826	, DUSP22, 1 more genes
nsv4371881	copy number variation	52	nstd173	human		GRCh37 chr17: 44,212,836-44,292,754 , GRCh38.p12 chr17: 46,135,470-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,577-917,561	KANSL1, KANSL1-AS1, 1 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
nsv4385515	copy number variation	6	nstd173	human		GRCh37 chr11: 58,811,241-58,854,985 , GRCh38.p12 chr11: 59,043,768-59,087,512	GLYATL1B, LOC105369315, 2 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
nsv4378397	copy number variation	79	nstd173	human		GRCh37 chr12: 11,216,817-11,247,388 , GRCh38.p12 chr12: 11,064,218-11,094,789	TAS2R64P, TAS2R43, 3 more genes
nsv4377904	copy number variation	28	nstd173	human		GRCh37 chr19: 20,596,118-20,720,868 , GRCh38.p12 chr19: 20,413,312-20,538,062	ZNF826P, ZNF737, 4 more genes
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4372108	copy number variation	2	nstd173	human		GRCh37 chr19: 22,341,905-23,207,386 , GRCh38.p12 chr19: 22,159,103-23,024,584	ZNF728, ZNF492, 36 more genes

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