1-0859-003 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
nsv4371561	copy number variation	3	nstd173	human		GRCh37 chr14: 47,696,247-47,717,503 , GRCh38.p12 chr14: 47,227,044-47,248,300	MDGA2
nsv4370897	copy number variation	108	nstd173	human		GRCh37 chr13: 57,758,269-57,778,367 , GRCh38.p12 chr13: 57,184,135-57,204,233	MTCO2P3
nsv4376485	copy number variation	50	nstd173	human		GRCh37 chr3: 173,239,853-173,300,180 , GRCh38.p12 chr3: 173,522,063-173,582,390	NLGN1
nsv4375141	copy number variation	7	nstd173	human		GRCh37 chr8: 39,230,324-39,386,964 , GRCh38.p12 chr8: 39,372,805-39,529,445	ADAM5, ADAM3A
nsv4368257	copy number variation	154	nstd173	human		GRCh37 chr11: 55,374,147-55,453,008 , GRCh38.p12 chr11: 55,606,671-55,685,532	OR4V1P, OR4P1P, 3 more genes
nsv4372499	copy number variation	1	nstd173	human		GRCh37 chr17: 19,494,953-19,543,162 , GRCh38.p12 chr17: 19,591,640-19,639,849	SLC47A1P1, MTCO1P39, 3 more genes
nsv4366415	copy number variation	1	nstd173	human		GRCh37 chr12: 8,004,412-8,142,625 , GRCh38.p12 chr12: 7,851,816-7,990,029	RPS20P29, LOC100130582, 3 more genes
nsv4381902	copy number variation	86	nstd173	human		GRCh37 chr17: 44,187,492-44,292,754 , GRCh38.p12 chr17: 46,110,126-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 812,225-917,561	LOC107985027, KANSL1-AS1, 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
nsv4369175	copy number variation	28	nstd173	human		GRCh37 chr12: 11,220,827-11,251,668 , GRCh38.p12 chr12: 11,068,228-11,099,069	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4372679	copy number variation	125	nstd173	human		GRCh37 chr14: 74,001,111-74,029,899 , GRCh38.p12 chr14: 73,534,407-73,563,195	HEATR4, ACOT1, 1 more genes
nsv4387296	copy number variation	3	nstd173	human		GRCh37 chr6: 31,359,886-31,480,958 , GRCh38.p12 chr6: 31,392,109-31,513,181	MICB, HCP5, 6 more genes
nsv4373995	copy number variation	15	nstd173	human		GRCh37 chr6: 29,841,021-29,921,751 , GRCh38.p12 chr6: 29,873,244-29,953,974	HCG4B, HCP5B, 12 more genes
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	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
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
nsv4368463	copy number variation	9	nstd173	human		GRCh37 chr6: 168,333,308-168,611,331 , GRCh38.p12 chr6: 167,932,628-168,210,651	AFDN, KIF25, 6 more genes

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