SP54286 AND nstd71 - 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
nsv909834	copy number variation	44	nstd71	human		NCBI36 chr18: 64,892,426-64,909,808 , GRCh37.p13 chr18: 66,741,446-66,758,828 , GRCh38.p12 chr18: 69,074,209-69,091,591	CCDC102B
nsv890754	copy number variation	920	nstd71	human		NCBI36 chr8: 39,350,791-39,509,376 , GRCh37.p13 chr8: 39,231,634-39,390,219 , GRCh38.p12 chr8: 39,374,115-39,532,700	ADAM5, ADAM3A
nsv873597	copy number variation	3	nstd71	human		NCBI36 chr2: 4,090,913-4,616,289 , GRCh37.p13 chr2: 4,113,038-4,638,414 , GRCh38.p12 chr2: 4,065,447-4,590,824	LOC105373397, LOC107985841, 1 more genes
nsv879310	copy number variation	1929	nstd71	human		NCBI36 chr4: 69,076,346-69,179,871 , GRCh37.p13 chr4: 69,393,751-69,497,276 , GRCh38.p12 chr4: 68,528,033-68,631,558	LOC100422402, LOC100132651, 2 more genes
nsv872053	copy number variation	32	nstd71	human		NCBI36 chr1: 103,999,836-104,070,228 , GRCh37.p13 chr1: 104,198,313-104,268,705 , GRCh38.p12 chr1: 103,655,691-103,726,083	AMY1B, LOC105378878, 2 more genes
nsv902761	copy number variation	101	nstd71	human		NCBI36 chr15: 19,031,743-19,212,282 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15: 20,729,748-21,258,351	POTEB2, MIR5701-1, 22 more genes
nsv890262	copy number variation	47	nstd71	human		NCBI36 chr8: 7,575,048-7,820,326 , GRCh37.p13 chr8: 7,537,638-7,782,916 , GRCh38.p12 chr8: 7,680,116-7,925,394 , GRCh38.p12 chr8\|NW_018654717.1: 5,303,324-5,513,617	DEFB103A, DEFB105B, 39 more genes
nsv890161	copy number variation	90	nstd71	human		NCBI36 chr8: 7,242,915-7,459,302 , GRCh37.p13 chr8: 7,255,505-7,471,892 , GRCh38.p12 chr8\|NT_187570.1: 81,014-297,473 , GRCh38.p12 chr8: 7,397,983-7,614,370	FAM90A22, FAM90A21P, 17 more genes
nsv874174	copy number variation	1	nstd71	human		NCBI36 chr2: 56,555,999-56,615,502 , GRCh37.p13 chr2: 56,702,495-56,761,998 , GRCh38.p12 chr2: 56,475,360-56,534,863	0
nsv895538	copy number variation	101	nstd71	human		NCBI36 chr10: 58,562,281-58,608,558 , GRCh37.p13 chr10: 58,892,275-58,938,552 , GRCh38.p12 chr10: 57,132,515-57,178,792	0
nsv903069	copy number variation	24	nstd71	human		NCBI36 chr15: 19,341,464-19,448,462 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr15\|NT_187602.1: 203,114-310,060 , GRCh38.p12 chr15\|NT_187382.1: 172,363-279,309	VN1R60P, NF1P9, 10 more genes

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SP54286 AND nstd71 (12)
dbVar
Homo sapiens family with sequence similarity 110 member D (FAM110D), mRNA
Homo sapiens family with sequence similarity 110 member D (FAM110D), mRNA
gi|1519246101|ref|NM_024869.3|

Nucleotide
RecName: Full=Protein FAM110D
RecName: Full=Protein FAM110D
gi|74751367|sp|Q8TAY7.1|F110D_HUMAN

Protein

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