2-0129-002 AND nstd173 - dbVar - NCBI

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Items: 19

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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
nsv4378288	copy number variation	15	nstd173	human		GRCh37 chr6: 78,969,092-79,041,720 , GRCh38.p12 chr6: 78,259,375-78,332,003	LOC105377865
nsv4370586	copy number variation	3	nstd173	human		GRCh37 chr8: 3,618,749-3,649,617 , GRCh38.p12 chr8: 3,761,227-3,792,095	CSMD1
nsv4385917	copy number variation	155	nstd173	human		GRCh37 chr2: 98,138,417-98,162,188 , GRCh38.p12 chr2: 97,521,954-97,545,725	ANKRD36B
nsv4384672	copy number variation	1	nstd173	human		GRCh37 chr10: 37,448,929-37,479,218 , GRCh38.p12 chr10: 37,160,001-37,190,290	ANKRD30A
nsv4386881	copy number variation	41	nstd173	human		GRCh37 chr7: 142,827,954-142,891,721 , GRCh38.p12 chr7: 143,130,861-143,194,628	PIP, TAS2R39
nsv4375646	copy number variation	78	nstd173	human		GRCh37 chr1: 72,762,663-72,810,925 , GRCh38.p12 chr1: 72,296,980-72,345,242 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,467	LOC105378797, RPL31P12
nsv4388281	copy number variation	1	nstd173	human		GRCh37 chr17: 21,434,480-21,508,930 , GRCh38.p12 chr17: 21,531,219-21,605,664	LINC02693, LOC100533653
nsv4376723	copy number variation	40	nstd173	human		GRCh37 chr12: 8,558,475-8,584,702 , GRCh38.p12 chr12: 8,405,879-8,432,106	OR7E140P, OR7E148P
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
nsv4373364	copy number variation	3	nstd173	human		GRCh37 chrY: 7,008,465-7,249,025 , GRCh38.p12 chrY: 7,140,424-7,380,984	PRKY, RNU6-941P, 1 more genes
nsv4386586	copy number variation	1	nstd173	human		GRCh37 chr14: 70,778,156-70,860,741 , GRCh38.p12 chr14: 70,311,439-70,394,024	SYNJ2BP-COX16, LOC101928046, 3 more genes
nsv4374589	copy number variation	1	nstd173	human		GRCh37 chr4: 39,761,240-39,811,548 , GRCh38.p12 chr4: 39,759,620-39,809,928	RN7SL558P, UBE2K, 1 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
nsv4367001	copy number variation	197	nstd173	human		GRCh37 chr14: 74,001,111-74,024,031 , GRCh38.p12 chr14: 73,534,407-73,557,327	NT5CP2, ACOT1, 1 more genes
nsv4386828	copy number variation	67	nstd173	human		GRCh37 chr19: 20,596,118-20,716,388 , GRCh38.p12 chr19: 20,413,312-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4365532	copy number variation	28	nstd173	human		GRCh37 chr18: 65,846,227-65,898,107 , GRCh38.p12 chr18: 68,178,990-68,230,870	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
nsv4370946	copy number variation	301	nstd173	human		GRCh37 chr16: 34,466,691-34,755,828 , GRCh38.p12 chr16: 35,232,320-35,521,457	RARRES2P7, AGGF1P9, 26 more genes

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