1-0696-004 AND nstd173 - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4378292	copy number variation	1	nstd173	human		GRCh37 chr20: 14,408,090-14,464,761 , GRCh38.p12 chr20: 14,427,444-14,484,115	MACROD2
nsv4368023	copy number variation	1	nstd173	human		GRCh37 chr7: 111,066,013-111,101,898 , GRCh38.p12 chr7: 111,425,957-111,461,842	IMMP2L
nsv4384438	copy number variation	5	nstd173	human		GRCh37 chr11: 21,183,993-21,212,091 , GRCh38.p12 chr11: 21,162,447-21,190,545	NELL1
nsv4368430	copy number variation	10	nstd173	human		GRCh37 chr17: 6,107,113-6,133,978 , GRCh38.p12 chr17: 6,203,793-6,230,658	RNU6-1264P
nsv4373339	copy number variation	53	nstd173	human		GRCh37 chrX: 150,698,534-150,722,241 , GRCh38.p12 chrX: 151,530,062-151,553,769	LOC105373367
nsv4383950	copy number variation	1	nstd173	human		GRCh37 chr2: 21,429,674-21,467,478 , GRCh38.p12 chr2: 21,206,802-21,244,606	LOC105374317
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
nsv4381858	copy number variation	13	nstd173	human		GRCh37 chr4: 69,435,889-69,540,417 , GRCh38.p12 chr4: 68,570,171-68,674,699	UGT2B15, LOC100422402, 3 more genes
nsv4384776	copy number variation	87	nstd173	human		GRCh37 chr19: 52,131,800-52,154,905 , GRCh38.p12 chr19: 51,628,547-51,651,652	SIGLEC5, SIGLEC14, 1 more genes
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4382082	copy number variation	609	nstd173	human		GRCh37 chr11: 55,374,019-55,442,305 , GRCh38.p12 chr11: 55,606,543-55,674,829	OR4C6, OR4P4, 2 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4379563	copy number variation	7	nstd173	human		GRCh37 chr17: 44,213,649-44,784,639 , GRCh38.p12 chr17: 46,136,283-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 838,389-1,226,699	FAM215B, LOC100132570, 14 more genes
nsv4368887	copy number variation	2	nstd173	human		GRCh37 chr21: 24,848,615-24,883,646 , GRCh38.p12 chr21: 23,476,296-23,511,327	0
nsv4382973	copy number variation	317	nstd173	human		GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428	BTNL3, LOC100128762, 4 more genes
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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