14-0119-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4373171	copy number variation	2	nstd173	human		GRCh37 chr12: 18,226,577-18,316,993 , GRCh38.p12 chr12: 18,073,643-18,164,059	RERGL
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
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
nsv4380672	copy number variation	18	nstd173	human		GRCh37 chrX: 102,808,754-102,831,104 , GRCh38.p12 chrX: 103,553,826-103,576,176	TCEAL4, LINC02589
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
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
nsv4374463	copy number variation	7	nstd173	human		GRCh37 chr14: 74,001,111-74,038,550 , GRCh38.p12 chr14: 73,534,407-73,571,846	ACOT1, ACOT2, 3 more genes
nsv4382558	copy number variation	13	nstd173	human		GRCh37 chr12: 11,216,817-11,247,376 , GRCh38.p12 chr12: 11,064,218-11,094,777	PRH1-TAS2R14, PRH1-PRR4, 3 more genes
nsv4381531	copy number variation	237	nstd173	human		GRCh37 chr2: 34,701,643-34,737,163 , GRCh38.p12 chr2: 34,476,576-34,512,096	0
nsv4365139	copy number variation	2	nstd173	human		GRCh37 chr1: 192,874,651-192,897,363 , GRCh38.p12 chr1: 192,905,521-192,928,233	0
nsv4369957	copy number variation	137	nstd173	human		GRCh37 chr10: 46,966,546-47,149,423 , GRCh38.p12 chr10: 46,400,340-46,583,071	GPRIN2, , 5 more genes
nsv4371136	copy number variation	1	nstd173	human		GRCh37 chr1: 167,491,881-168,643,013 , GRCh38.p12 chr1: 167,522,644-168,673,775	RPL7AP21, RCSD1, 29 more genes
nsv4387573	copy number variation	172	nstd173	human		GRCh37 chr11: 54,701,632-54,757,928 , GRCh38.p12 chr11: 54,934,156-54,990,452	0
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0
nsv4387382	copy number variation	84	nstd173	human		GRCh37 chr5: 57,326,026-57,349,970 , GRCh38.p12 chr5: 58,030,199-58,054,143	0

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