2-1688-002 AND nstd173 - dbVar - NCBI

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Items: 11

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4371450	copy number variation	57	nstd173	human		GRCh37 chr12: 2,235,941-2,257,920 , GRCh38.p12 chr12: 2,126,775-2,148,754 , GRCh38.p12 chr12\|NW_018654718.1: 468,919-490,898	LOC107984131, CACNA1C
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
nsv4373419	copy number variation	5	nstd173	human		GRCh37 chr6: 253,308-384,754 , GRCh38.p12 chr6: 253,308-384,754	DUSP22, , 1 more genes
nsv4385846	copy number variation	1	nstd173	human		GRCh37 chr18: 2,965,319-3,062,944 , GRCh38.p12 chr18: 2,965,321-3,062,946	SNRPCP4, LOC105371963, 1 more genes
nsv4382148	copy number variation	1	nstd173	human		GRCh37 chr16: 75,533,670-75,574,798 , GRCh38.p12 chr16: 75,499,772-75,540,900	CHST5, TMEM231, 1 more genes
nsv4381596	copy number variation	144	nstd173	human		GRCh37 chr14: 74,001,123-74,024,031 , GRCh38.p12 chr14: 73,534,419-73,557,327	HEATR4, NT5CP2, 1 more genes
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4368892	copy number variation	173	nstd173	human		GRCh37 chr14: 106,530,472-106,693,442 , GRCh38.p12 chr14: 106,074,229-106,236,829 , GRCh38.p12 chr14\|NT_187600.1: 541,998-704,598	LOC105370700, IGHV3-19, 19 more genes
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

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