214102 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
nsv4368029	copy number variation	55	nstd173	human		GRCh37 chr10: 68,077,579-68,122,519 , GRCh38.p12 chr10: 66,317,821-66,362,761	CTNNA3
nsv4368807	copy number variation	30	nstd173	human		GRCh37 chr20: 1,560,774-1,598,093 , GRCh38.p12 chr20: 1,580,128-1,617,447	SIRPB1
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4377726	copy number variation	23	nstd173	human		GRCh37 chr6: 55,823,233-55,843,659 , GRCh38.p12 chr6: 55,958,435-55,978,861	LOC107986539
nsv4374624	copy number variation	1	nstd173	human		GRCh37 chr2: 230,792,698-230,818,673 , GRCh38.p12 chr2: 229,927,982-229,953,957	RNU6-964P, FBXO36
nsv4378360	copy number variation	3	nstd173	human		GRCh37 chr8: 39,225,875-39,386,964 , GRCh38.p12 chr8: 39,368,356-39,529,445	ADAM5, ADAM3A
nsv4377524	copy number variation	13	nstd173	human		GRCh37 chrX: 62,461,600-62,505,606 , GRCh38.p12 chrX: 63,241,721-63,285,729	LOC100533730, LOC105377212
nsv4383263	copy number variation	11	nstd173	human		GRCh37 chr6: 253,308-387,482 , GRCh38.p12 chr6: 253,308-387,482	DUSP22, , 1 more genes
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
nsv4380110	copy number variation	3	nstd173	human		GRCh37 chr1: 1,616,990-1,652,905 , GRCh38.p12 chr1: 1,685,551-1,721,466	MMP23A, CDK11A, 1 more genes
nsv4371329	copy number variation	1	nstd173	human		GRCh37 chr4: 60,200,228-61,769,478 , GRCh38.p12 chr4: 59,334,510-60,903,760	LOC100421808, LINC02496, 1 more genes
nsv4382126	copy number variation	56	nstd173	human		GRCh37 chr11: 55,386,384-55,442,305 , GRCh38.p12 chr11: 55,618,908-55,674,829	OR4P4, OR4S2, 2 more genes
nsv4368241	copy number variation	217	nstd173	human		GRCh37 chr17: 34,437,482-34,477,480 , GRCh38.p12 chr17: 36,110,089-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,186-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,010-385,008	LOC100419980, LOC101927369, 3 more genes
nsv4373711	copy number variation	238	nstd173	human		GRCh37 chr14: 74,001,111-74,031,034 , GRCh38.p12 chr14: 73,534,407-73,564,330	NT5CP2, HEATR4, 1 more genes
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
nsv4383557	copy number variation	2	nstd173	human		GRCh37 chr14: 22,424,059-22,995,095 , GRCh38.p12 chr14: 21,955,835-22,526,126	TRAV38-1, TRAJ34, 92 more genes
nsv4387089	copy number variation	69	nstd173	human		GRCh37 chr7: 142,342,271-142,493,638 , GRCh38.p12 chr7: 142,634,755-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV21-1, TRB, 21 more genes
nsv4370415	copy number variation	102	nstd173	human		GRCh37 chr7: 38,294,983-38,394,857 , GRCh38.p12 chr7: 38,255,382-38,355,256	TRGV5, TRGV7, 19 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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