M2324 AND nstd157 - 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
nsv3317854	copy number variation	1	nstd157	human		GRCh37 chr14: 42,971,788-43,086,390 , GRCh38.p12 chr14: 42,502,585-42,617,187	LOC100420765
nsv3318516	copy number variation	22	nstd157	human		GRCh37 chr13: 64,225,427-64,236,288 , GRCh38.p12 chr13: 63,651,294-63,662,155	LOC105370236
nsv3317983	copy number variation	1	nstd157	human		GRCh37 chr5: 112,264,968-112,272,250 , GRCh38.p12 chr5: 112,929,271-112,936,553	LOC105379123
nsv3318140	copy number variation	5	nstd157	human		GRCh37 chr4: 113,045,230-113,050,302 , GRCh38.p12 chr4: 112,124,074-112,129,146	LOC105377370
nsv3317107	copy number variation	1	nstd157	human		GRCh37 chr4: 21,218,970-21,267,896 , GRCh38.p12 chr4: 21,217,347-21,266,273	KCNIP4
nsv3318325	copy number variation	1	nstd157	human		GRCh37 chr2: 77,977,262-78,001,566 , GRCh38.p12 chr2: 77,750,136-77,774,440	LOC101927967
nsv3317638	copy number variation	9	nstd157	human		GRCh37 chr10: 56,448,886-56,468,486 , GRCh38.p12 chr10: 54,689,126-54,708,726	PCDH15
nsv3318955	copy number variation	1	nstd157	human		GRCh38.p12 chr12: 50,957,066-50,982,186 , GRCh37 chr12: 51,350,849-51,375,969	SLC11A2, HIGD1C
nsv3318042	copy number variation	23	nstd157	human		GRCh38.p12 chr19: 53,015,494-53,049,043 , GRCh37 chr19: 53,518,747-53,552,296	ERVV-1, ERVV-2
nsv3318457	copy number variation	10	nstd157	human		GRCh38.p12 chr6: 266,035-379,638 , GRCh37 chr6: 266,035-379,638	DUSP22, , 1 more genes
nsv3317392	copy number variation	23	nstd157	human		GRCh38.p12 chr4: 68,527,638-68,623,755 , GRCh37 chr4: 69,393,356-69,489,473	UGT2B17, LOC100132651, 1 more genes
nsv3318442	copy number variation	7	nstd157	human		GRCh38.p12 chr16: 33,788,492-33,828,788 , GRCh37 chr16: 33,590,959-33,631,255	IGHV3OR16-12, LOC342443, 1 more genes
nsv3318385	copy number variation	1	nstd157	human		GRCh38.p12 chr16: 8,642,171-8,689,741 , GRCh37 chr16: 8,736,028-8,783,598	ABAT, METTL22, 1 more genes
nsv3317168	copy number variation	1	nstd157	human		GRCh38.p12 chr16: 8,698,200-8,736,969 , GRCh37 chr16: 8,792,057-8,830,826	ABAT, RNU7-63P, 1 more genes
nsv3318316	copy number variation	72	nstd157	human		GRCh37 chr14: 41,615,868-41,661,685 , GRCh38.p12 chr14: 41,146,665-41,192,482	0
nsv3317289	copy number variation	24	nstd157	human		GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797	0
nsv3318719	copy number variation	1	nstd157	human		GRCh37 chr14: 43,108,456-43,118,925 , GRCh38.p12 chr14: 42,639,253-42,649,722	0
nsv3318819	copy number variation	7	nstd157	human		GRCh37 chr5: 98,090,590-98,096,735 , GRCh38.p12 chr5: 98,754,886-98,761,031	0
nsv3318671	copy number variation	17	nstd157	human		GRCh37 chr5: 180,176,005-180,195,526 , GRCh38.p12 chr5: 180,749,005-180,768,526	0

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