"nstd177"[study] AND "deletion"[variant_type] - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4449713	copy number variation	1	nstd177	human		GRCh37 chr4: 144,912,872-145,016,256 , GRCh38.p12 chr4: 143,991,719-144,095,103	GYPB, LOC105377460
nsv4449708	copy number variation	1	nstd177	human		GRCh37 chr4: 144,752,739-144,954,739 , GRCh38.p12 chr4: 143,831,586-144,033,586	GYPB, GYPE, 3 more genes
nsv4449709	copy number variation	1	nstd177	human		GRCh37 chr4: 144,755,739-144,878,739 , GRCh38.p12 chr4: 143,834,586-143,957,586	GYPE, LOC100420464, 2 more genes
nsv4449724	copy number variation	1	nstd177	human		GRCh37 chr4: 144,800,739-144,922,739 , GRCh38.p12 chr4: 143,879,586-144,001,586	GYPB, GYPE, 3 more genes
nsv4449714	copy number variation	1	nstd177	human		GRCh37 chr4: 144,925,739-145,045,739 , GRCh38.p12 chr4: 144,004,586-144,124,586	GYPA, GYPB, 2 more genes
nsv4449719	copy number variation	1	nstd177	human		GRCh37 chr4: 144,882,739-144,987,739 , GRCh38.p12 chr4: 143,961,586-144,066,586	GYPB, LOC101927636, 1 more genes
nsv4449722	copy number variation	1	nstd177	human		GRCh37 chr4: 144,780,111-144,901,334 , GRCh38.p12 chr4: 143,858,958-143,980,181	GYPE, LOC100420464, 2 more genes
nsv4449716	copy number variation	1	nstd177	human		GRCh37 chr4: 144,835,143-144,945,517 , GRCh38.p12 chr4: 143,913,990-144,024,364	GYPB, LOC101927636, 1 more genes
nsv4449707	copy number variation	1	nstd177	human		GRCh37 chr4: 144,750,739-144,960,739 , GRCh38.p12 chr4: 143,829,586-144,039,586	GYPB, GYPE, 4 more genes
nsv4449721	copy number variation	1	nstd177	human		GRCh37 chr4: 144,780,045-145,004,212 , GRCh38.p12 chr4: 143,858,892-144,083,059	GYPB, GYPE, 4 more genes

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