OCD160-0625-4932-3 AND nstd173 - dbVar - NCBI

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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
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
nsv4374527	copy number variation	116	nstd173	human		GRCh37 chr2: 98,118,199-98,162,188 , GRCh38.p12 chr2: 97,501,736-97,545,725	ANKRD36B
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
nsv4367142	copy number variation	135	nstd173	human		GRCh37 chr12: 2,235,941-2,259,954 , GRCh38.p12 chr12: 2,126,775-2,150,788 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-492,932	LOC107984131, CACNA1C
nsv4365709	copy number variation	2	nstd173	human		GRCh37 chrX: 134,754,594-134,802,928 , GRCh38.p12 chrX: 135,620,669-135,669,213	SAGE4P, SAGE3P
nsv4376403	copy number variation	119	nstd173	human		GRCh37 chr19: 53,517,242-53,553,087 , GRCh38.p12 chr19: 53,013,989-53,049,834	ERVV-1, ERVV-2
nsv4379834	copy number variation	1	nstd173	human		GRCh37 chr11: 89,508,090-89,551,714 , GRCh38.p12 chr11: 89,774,922-89,818,546	TRIM49, TRIM64DP, 2 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
nsv4370014	copy number variation	6	nstd173	human		GRCh37 chr17: 44,213,637-44,276,618 , GRCh38.p12 chr17: 46,136,271-46,199,252 , GRCh38.p12 chr17\|NT_187663.1: 838,377-901,356	KANSL1, LOC107985027, 1 more genes
nsv4383892	copy number variation	82	nstd173	human		GRCh37 chr4: 69,435,901-69,485,839 , GRCh38.p12 chr4: 68,570,183-68,620,121	LOC100132651, LOC100422402, 1 more genes
nsv4370840	copy number variation	154	nstd173	human		GRCh37 chr12: 11,222,368-11,247,388 , GRCh38.p12 chr12: 11,069,769-11,094,789	TAS2R43, TAS2R64P, 3 more genes
nsv4376368	copy number variation	168	nstd173	human		GRCh37 chr6: 67,009,023-67,048,629 , GRCh38.p12 chr6: 66,299,130-66,338,736	0
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
nsv4367791	copy number variation	5	nstd173	human		GRCh37 chr22: 25,656,238-25,911,115 , GRCh38.p12 chr22: 25,260,271-25,515,148	CRYBB2P1, LRP5L, 4 more genes
nsv4372393	copy number variation	30	nstd173	human		GRCh37 chr11: 55,363,327-55,452,996 , GRCh38.p12 chr11: 55,595,851-55,685,520	OR4P1P, OR4P4, 4 more genes
nsv4366041	copy number variation	13	nstd173	human		GRCh37 chr14: 22,462,737-22,974,280 , GRCh38.p12 chr14: 21,994,497-22,505,293	TRAV29DV5, TRAJ48, 71 more genes
nsv4365850	copy number variation	1	nstd173	human		GRCh37 chr7: 142,230,575-142,475,287 , GRCh38.p12 chr7\|NT_187562.1: 622,348-792,624	TRBV27, TRBV24-1, 19 more genes
nsv4387680	copy number variation	51	nstd173	human		GRCh37 chr7: 38,294,983-38,378,483 , GRCh38.p12 chr7: 38,255,382-38,338,882	TRGV6, TRGJ1, 15 more genes
nsv4381956	copy number variation	239	nstd173	human		GRCh37 chr5: 57,326,026-57,351,813 , GRCh38.p12 chr5: 58,030,199-58,055,986	0

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