5-1000-003 AND nstd173 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4377929	copy number variation	15	nstd173	human		GRCh37 chr20: 14,768,903-14,823,472 , GRCh38.p12 chr20: 14,788,257-14,842,826	MACROD2
nsv4388100	copy number variation	1	nstd173	human		GRCh37 chr15: 94,138,206-94,158,318 , GRCh38.p12 chr15: 93,594,977-93,615,089	LOC107983974
nsv4374158	copy number variation	106	nstd173	human		GRCh37 chr3: 128,380,595-128,412,365 , GRCh38.p12 chr3: 128,661,752-128,693,522	POU5F1P6
nsv4382074	copy number variation	18	nstd173	human		GRCh37 chr2: 98,138,419-98,162,176 , GRCh38.p12 chr2: 97,521,956-97,545,713	ANKRD36B
nsv4375939	copy number variation	1	nstd173	human		GRCh37 chr21: 27,181,191-27,252,173 , GRCh38.p12 chr21: 25,808,880-25,879,862	LOC105372756, APP
nsv4371450	copy number variation	57	nstd173	human		GRCh37 chr12: 2,235,941-2,257,920 , GRCh38.p12 chr12: 2,126,775-2,148,754 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-490,898	LOC107984131, CACNA1C
nsv4372579	copy number variation	26	nstd173	human		GRCh37 chr5: 180,374,484-180,430,801 , GRCh38.p12 chr5: 180,947,484-181,003,801	BTNL8, LOC100128762, 3 more genes
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 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
nsv4365437	copy number variation	76	nstd173	human		GRCh37 chr17: 34,440,083-34,477,480 , GRCh38.p12 chr17: 36,112,690-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,787-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,611-385,008	LOC100419980, LOC101927369, 2 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
nsv4373636	copy number variation	20	nstd173	human		GRCh37 chr19: 24,457,025-24,504,428 , GRCh38.p12 chr19: 24,274,223-24,321,626	0
nsv4374519	copy number variation	45	nstd173	human		GRCh37 chr13: 69,238,142-69,264,684 , GRCh38.p12 chr13: 68,664,010-68,690,552	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
nsv4384179	copy number variation	1	nstd173	human		GRCh37 chr15: 43,845,462-43,936,960 , GRCh38.p12 chr15: 43,553,264-43,644,762	RNU6-554P, CATSPER2, 5 more genes
nsv4366283	copy number variation	6	nstd173	human		GRCh37 chr12: 11,215,194-11,247,388 , GRCh38.p12 chr12: 11,062,595-11,094,789	TAS2R43, TAS2R46, 4 more genes
nsv4369096	copy number variation	1	nstd173	human		GRCh37 chr2: 110,925,256-111,397,799 , GRCh38.p12 chr2: 110,167,679-110,640,222	LOC105373551, LOC107985776, 18 more genes
nsv4384206	copy number variation	78	nstd173	human		GRCh37 chr5: 57,326,267-57,351,813 , GRCh38.p12 chr5: 58,030,440-58,055,986	0

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