14-0260-003 AND nstd173 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387332	copy number variation	1	nstd173	human		GRCh37 chr3: 41,093,451-41,150,723 , GRCh38.p12 chr3: 41,051,960-41,109,232	LOC105377045
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
nsv4388442	copy number variation	2	nstd173	human		GRCh37 chr2: 217,284,892-217,317,765 , GRCh38.p12 chr2: 216,420,169-216,453,042	SMARCAL1
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4383195	copy number variation	1	nstd173	human		GRCh37 chr16: 7,101,376-7,131,548 , GRCh38.p12 chr16: 7,051,375-7,081,547	LOC105371068, RBFOX1
nsv4376755	copy number variation	329	nstd173	human		GRCh37 chr14: 74,001,122-74,024,031 , GRCh38.p12 chr14: 73,534,418-73,557,327	ACOT1, NT5CP2, 1 more genes
nsv4382978	copy number variation	2	nstd173	human		GRCh37 chr2: 217,186,190-217,250,099 , GRCh38.p12 chr2: 216,321,467-216,385,376	SMARCAL1-AS1, MARCHF4, 1 more genes
nsv4373687	copy number variation	26	nstd173	human		GRCh37 chr6: 257,340-302,261 , GRCh38.p12 chr6: 257,340-302,261	, , 1 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
nsv4371902	copy number variation	41	nstd173	human		GRCh37 chr6: 67,004,973-67,048,629 , GRCh38.p12 chr6: 66,295,080-66,338,736	0
nsv4372192	copy number variation	1	nstd173	human		GRCh37 chr8: 53,353,236-53,893,517 , GRCh38.p12 chr8: 52,440,676-52,980,957	RB1CC1, LOC101060191, 4 more genes
nsv4369957	copy number variation	137	nstd173	human		GRCh37 chr10: 46,966,546-47,149,423 , GRCh38.p12 chr10: 46,400,340-46,583,071	GPRIN2, , 5 more genes
nsv4382474	copy number variation	59	nstd173	human		GRCh37 chr17: 44,188,310-44,784,639 , GRCh38.p12 chr17: 46,110,944-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 813,043-1,226,699	RN7SL199P, ARL17A, 14 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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