7-0177-003 AND nstd173 - dbVar - NCBI

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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
nsv4375716	copy number variation	91	nstd173	human		GRCh37 chr3: 165,041,535-165,085,386 , GRCh38.p12 chr3: 165,323,747-165,367,598	LINC01322
nsv4379044	copy number variation	44	nstd173	human		GRCh37 chr20: 1,560,549-1,593,836 , GRCh38.p12 chr20: 1,579,903-1,613,190	SIRPB1
nsv4367151	copy number variation	67	nstd173	human		GRCh37 chr11: 18,941,197-18,961,600 , GRCh38.p12 chr11: 18,919,650-18,940,053	MRGPRX1
nsv4374170	copy number variation	1	nstd173	human		GRCh37 chr7: 75,351,138-75,378,713 , GRCh38.p12 chr7: 75,721,820-75,749,395	HIP1
nsv4370537	copy number variation	8	nstd173	human		GRCh37 chr12: 11,503,225-11,564,511 , GRCh38.p12 chr12: 11,350,291-11,411,577	PRB1, PRB2
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4376272	copy number variation	17	nstd173	human		GRCh37 chr1: 248,753,184-248,795,288 , GRCh38.p12 chr1: 248,589,883-248,631,987	OR2T11, OR2T10
nsv4374759	copy number variation	3	nstd173	human		GRCh37 chr19: 41,345,315-41,380,933 , GRCh38.p12 chr19: 40,839,410-40,875,028	CYP2A7, CYP2A6
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 1 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
nsv4384024	copy number variation	30	nstd173	human		GRCh37 chr17: 44,187,492-44,288,454 , GRCh38.p12 chr17: 46,110,126-46,211,088 , GRCh38.p12 chr17\|NT_187663.1: 812,225-913,262	LOC107985027, KANSL1-AS1, 1 more genes
nsv4375664	copy number variation	26	nstd173	human		GRCh37 chr6: 254,254-294,712 , GRCh38.p12 chr6: 254,254-294,712	, , 1 more genes
nsv4384287	copy number variation	36	nstd173	human		GRCh37 chr17: 34,440,095-34,477,480 , GRCh38.p12 chr17: 36,112,702-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,799-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,623-385,008	LOC107985055, LOC100419980, 2 more genes
nsv4380515	copy number variation	77	nstd173	human		GRCh37 chr12: 8,558,475-8,594,982 , GRCh38.p12 chr12: 8,405,879-8,442,386	OR7E148P, OR7E149P, 1 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4376368	copy number variation	168	nstd173	human		GRCh37 chr6: 67,009,023-67,048,629 , GRCh38.p12 chr6: 66,299,130-66,338,736	0
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0

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7-0177-003 AND nstd173 (20)
dbVar
Taxonomy Links for Gene (Select 127816401) (1)
Taxonomy
Spata21 spermatogenesis associated 21 [Rattus norvegicus]
Spata21 spermatogenesis associated 21 [Rattus norvegicus]
Gene ID:366491

Gene
Gene Links for Protein (Select 81910741) (1)
Gene

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