CN169374[trait identifier] AND "ARUP Laboratories, Cytogenetics and Ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063532	GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3	ACP6, ADAM15 +263 more	Copy number gain	not specified	GPathogenic
Select item 3063521	GRCh37/hg19 1q24.2-31.1(chr1:167994071-187711459)x1	ABL2, ACBD6 +123 more	Copy number loss	not specified	GPathogenic
Select item 3063510	GRCh37/hg19 1q32.1(chr1:204864008-204929778)x1	NFASC	Copy number loss	not specified	GUncertain significance
Select item 3063499	GRCh37/hg19 1q44(chr1:246179295-246704479)x1	SMYD3, TFB2M	Copy number loss	not specified	GUncertain significance
Select item 3063488	GRCh37/hg19 1q43-44(chr1:243453390-245467768)x1	ADSS2, AKT3 +9 more	Copy number loss	not specified	GPathogenic
Select item 3063477	GRCh37/hg19 1q21.2(chr1:147186576-147334957)x3	GJA5	Copy number gain	not specified	GUncertain significance
Select item 3063466	GRCh37/hg19 1p12(chr1:119959511-119988221)x1	HSD3B2	Copy number loss	not specified	GUncertain significance
Select item 3063455	GRCh37/hg19 1p36.12(chr1:21722949-22021145)x3	ALPL, NBPF3 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063454	GRCh37/hg19 1p13.3-13.2(chr1:109700156-112176616)x1	ADORA3, AHCYL1 +48 more	Copy number loss	not specified	GUncertain significance
Select item 3063443	GRCh37/hg19 1q42.2-43(chr1:233813555-240578304)x1	ACTN2, ARID4B +24 more	Copy number loss	not specified	GPathogenic
Select item 3063432	GRCh37/hg19 1p31.1(chr1:72399667-72433308)x1	NEGR1	Copy number loss	not specified	GUncertain significance
Select item 3063421	GRCh37/hg19 1p12(chr1:119425396-120523902)x3	ADAM30, HAO2 +9 more	Copy number gain	not specified	GUncertain significance
Select item 3063410	GRCh37/hg19 1p32.1-31.3(chr1:59121165-62057570)x1	C1orf87, CYP2J2 +5 more	Copy number loss	not specified	GPathogenic
Select item 3063399	GRCh37/hg19 1p36.31-36.21(chr1:6330828-12910774)x1	AADACL3, AADACL4 +80 more	Copy number loss	not specified	GPathogenic
Select item 3063388	GRCh37/hg19 1q21.1(chr1:145452902-145557355)x3	ANKRD34A, ANKRD35 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063377	GRCh37/hg19 1q21.3(chr1:153354333-153703053)x3	CHTOP, ILF2 +16 more	Copy number gain	not specified	GUncertain significance
Select item 3063366	GRCh37/hg19 1p36.31(chr1:6810718-7036045)x1	CAMTA1	Copy number loss	not specified	GPathogenic
Select item 3063355	GRCh37/hg19 1p13.2(chr1:113095600-113554789)x3	CAPZA1, MOV10 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063344	GRCh37/hg19 1p36.22(chr1:10496415-10632298)x1	CENPS, CENPS-CORT +3 more	Copy number loss	not specified	GUncertain significance
Select item 3063343	GRCh37/hg19 1p36.32-36.23(chr1:4536962-7934520)x1	ACOT7, AJAP1 +23 more	Copy number loss	not specified	GPathogenic
Select item 3063332	GRCh37/hg19 1p13.3(chr1:109402942-109807574)x3	CELSR2, CFAP276 +7 more	Copy number gain	not specified	GUncertain significance
Select item 3063321	GRCh37/hg19 1q43(chr1:240407420-240835685)x3	FMN2, GREM2	Copy number gain	not specified	GUncertain significance
Select item 3063310	GRCh37/hg19 1p36.23(chr1:8403000-8480452)x3	RERE, SLC45A1	Copy number gain	not specified	GUncertain significance
Select item 3063299	GRCh37/hg19 1q42.3-43(chr1:236221501-237380903)x3	ACTN2, EDARADD +8 more	Copy number gain	not specified	GUncertain significance
Select item 3063288	GRCh37/hg19 1q23.1(chr1:157798293-157887020)x1	CD5L	Copy number loss	not specified	GUncertain significance
Select item 3063277	GRCh37/hg19 1p33(chr1:50250602-50400110)x1	AGBL4	Copy number loss	not specified	GUncertain significance
Select item 3063266	GRCh37/hg19 1q42.2(chr1:232523331-232565831)x3	SIPA1L2	Copy number gain	not specified	GUncertain significance
Select item 3063255	GRCh37/hg19 1p36.33-36.32(chr1:849466-4529103)x3	ACAP3, ACTRT2 +76 more	Copy number gain	not specified	GPathogenic
Select item 3063244	GRCh37/hg19 1p13.3(chr1:111167391-111232936)x3	KCNA2, KCNA3	Copy number gain	not specified	GUncertain significance
Select item 3063233	GRCh37/hg19 1p36.33-36.23(chr1:849466-8966102)x1	RNF207, RNF223 +108 more	Copy number loss	not specified	GPathogenic
Select item 3063232	GRCh37/hg19 1q44(chr1:245007762-245037711)x1	COX20, HNRNPU	Copy number loss	not specified	GPathogenic
Select item 3063221	GRCh37/hg19 1p31.3(chr1:63047044-64769540)x1	ALG6, ANGPTL3 +8 more	Copy number loss	not specified	GUncertain significance
Select item 3063210	GRCh37/hg19 1q43(chr1:237966553-240835685)x1	CHRM3, FMN2 +3 more	Copy number loss	not specified	GPathogenic
Select item 3063199	GRCh37/hg19 1q21.3-23.1(chr1:154302443-156868186)x1	ADAM15, ADAR +85 more	Copy number loss	not specified	GPathogenic
Select item 3063188	GRCh37/hg19 1q21.1-21.2(chr1:146106723-147844758)x3	ACP6, BCL9 +7 more	Copy number gain	not specified	GPathogenic
Select item 3063177	GRCh37/hg19 1q25.1-25.2(chr1:175999385-176105676)x1	COP1	Copy number loss	not specified	GUncertain significance
Select item 3063166	GRCh37/hg19 1p22.1-21.3(chr1:94304238-97280301)x3	ABCA4, ABCD3 +11 more	Copy number gain	not specified	GUncertain significance
Select item 3063155	GRCh37/hg19 1q25.3(chr1:183417292-183502236)x3	SMG7	Copy number gain	not specified	GUncertain significance
Select item 3063144	GRCh37/hg19 1q21.1(chr1:145406357-145430360)x1	HJV	Copy number loss	not specified	GUncertain significance
Select item 3063133	GRCh37/hg19 1q43-44(chr1:238681812-249224684)x3	OR2W3, OR6F1 +81 more	Copy number gain	not specified	GLikely pathogenic
Select item 3063122	GRCh37/hg19 1p36.11(chr1:27014190-27179034)x3	ARID1A, PIGV +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063121	GRCh37/hg19 1p34.1(chr1:45857175-46077062)x3	AKR1A1, MMACHC +3 more	Copy number gain	not specified	GUncertain significance
Select item 3063110	GRCh37/hg19 1q32.1(chr1:202261387-202375150)x3	LGR6, PPP1R12B +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063099	GRCh37/hg19 1p13.3(chr1:109255293-109812358)x3	AKNAD1, CELSR2 +10 more	Copy number gain	not specified	GUncertain significance
Select item 3063088	GRCh37/hg19 1q41(chr1:215576055-215927476)x3	KCTD3, USH2A	Copy number gain	not specified	GUncertain significance
Select item 3063077	GRCh37/hg19 1p34.1(chr1:44810778-45212378)x3	ARMH1, ERI3 +3 more	Copy number gain	not specified	GUncertain significance
Select item 3063066	GRCh37/hg19 1p36.33-36.31(chr1:1959612-5471235)x1	ACTRT2, AJAP1 +27 more	Copy number loss	not specified	GPathogenic
Select item 3063055	GRCh37/hg19 1p36.31(chr1:6727645-6854433)x1	CAMTA1, DNAJC11	Copy number loss	not specified	GPathogenic
Select item 3063044	GRCh37/hg19 1q43(chr1:240332313-240352790)x1	FMN2	Copy number loss	not specified	GUncertain significance
Select item 3063033	GRCh37/hg19 1p36.13(chr1:20058581-20169174)x1	RNF186, TMCO4	Copy number loss	not specified	GUncertain significance
Select item 3063022	GRCh37/hg19 1q25.1(chr1:173845743-173891648)x1	SERPINC1, ZBTB37	Copy number loss	not specified	GPathogenic
Select item 3063011	GRCh37/hg19 1p13.1-12(chr1:117338180-117990154)x1	CD101, MAN1A2 +4 more	Copy number loss	not specified	GUncertain significance
Select item 3063010	GRCh37/hg19 1p31.3(chr1:63885043-65190254)x1	ALG6, CACHD1 +5 more	Copy number loss	not specified	GPathogenic
Select item 3062999	GRCh37/hg19 1q21.1-21.2(chr1:146496425-147048600)x3	BCL9, CHD1L +2 more	Copy number gain	not specified	GUncertain significance
Select item 3062988	GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	ACP6, ADAM15 +315 more	Copy number gain	not specified	GPathogenic
Select item 3062977	GRCh37/hg19 1q21.1-21.2(chr1:146470887-147929115)x1	ACP6, BCL9 +6 more	Copy number loss	not specified	GPathogenic
Select item 3062966	GRCh37/hg19 1p31.1(chr1:82134940-82242495)x3		Copy number gain	not specified	GUncertain significance
Select item 3062955	GRCh37/hg19 1q32.1(chr1:199373229-204335027)x3	ADIPOR1, ADORA1 +58 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062944	GRCh37/hg19 1q25.3(chr1:183173518-183221795)x3	LAMC2, NMNAT2	Copy number gain	not specified	GUncertain significance
Select item 3062933	GRCh37/hg19 1p13.3(chr1:109367168-109429175)x3	AKNAD1, GPSM2	Copy number gain	not specified	GUncertain significance
Select item 3062922	GRCh37/hg19 1p32.2(chr1:57250058-57377172)x3	C8A, FYB2	Copy number gain	not specified	GUncertain significance
Select item 3062911	GRCh37/hg19 1p36.21(chr1:13922015-16013972)x1	AGMAT, CASP9 +13 more	Copy number loss	not specified	GUncertain significance
Select item 3062900	GRCh37/hg19 1q21.3(chr1:154089394-154912611)x3	ADAR, AQP10 +14 more	Copy number gain	not specified	GUncertain significance
Select item 3062899	GRCh37/hg19 1p21.3(chr1:98021778-98645029)x1	DPYD, MIR137	Copy number loss	not specified	GUncertain significance
Select item 3062888	GRCh37/hg19 1q21.1-21.2(chr1:146112080-147806677)x3	ACP6, BCL9 +7 more	Copy number gain	not specified	GPathogenic
Select item 3062877	GRCh37/hg19 1q42.13(chr1:228215364-229747702)x1	CCSAP, ABCB10 +21 more	Copy number loss	not specified	GPathogenic
Select item 3062866	GRCh37/hg19 1q21.1-21.2(chr1:146043713-147830830)x1	ACP6, BCL9 +8 more	Copy number loss	not specified	GPathogenic
Select item 3062855	GRCh37/hg19 1q25.1(chr1:173701568-173961992)x3	CENPL, DARS2 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3062844	GRCh37/hg19 1p31.1(chr1:70886158-71330939)x3	CTH, PTGER3	Copy number gain	not specified	GUncertain significance
Select item 3062833	GRCh37/hg19 1q25.1-25.2(chr1:174833865-176232490)x1	CACYBP, COP1 +5 more	Copy number loss	not specified	GUncertain significance
Select item 3062822	GRCh37/hg19 1p36.21-36.12(chr1:16194137-20561434)x1	ACTL8, AKR7A2 +58 more	Copy number loss	not specified	GPathogenic
Select item 3062811	GRCh37/hg19 1q21.1-21.2(chr1:146105170-147830830)x1	ACP6, BCL9 +7 more	Copy number loss	not specified	GPathogenic
Select item 3062800	GRCh37/hg19 1q25.1-25.2(chr1:175917018-176316555)x1	COP1	Copy number loss	not specified	GUncertain significance
Select item 3062789	GRCh37/hg19 1q21.1-21.2(chr1:146470887-147856007)x3	ACP6, BCL9 +6 more	Copy number gain	not specified	GPathogenic
Select item 3062788	GRCh37/hg19 1p35.1(chr1:33490421-33599915)x1	AK2, AZIN2	Copy number loss	not specified	GPathogenic
Select item 3062777	GRCh37/hg19 1q25.1-25.3(chr1:173162501-182702252)x3	ABL2, ACBD6 +52 more	Copy number gain	not specified	GPathogenic
Select item 3062766	GRCh37/hg19 1q23.3(chr1:161333263-161413937)x3	CFAP126, SDHC	Copy number gain	not specified	GUncertain significance
Select item 3062755	GRCh37/hg19 1p33-32.2(chr1:47493178-57042671)x3	ACOT11, AGBL4 +72 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062744	GRCh37/hg19 1p31.1(chr1:72126327-73436923)x3	NEGR1, NEGR1-IT1	Copy number gain	not specified	GUncertain significance
Select item 3062733	GRCh37/hg19 1p13.3-13.2(chr1:111277065-111804157)x1	CD53, CEPT1 +4 more	Copy number loss	not specified	GUncertain significance
Select item 3062722	GRCh37/hg19 1q21.1-21.2(chr1:146470887-147929323)x1	ACP6, BCL9 +6 more	Copy number loss	not specified	GPathogenic
Select item 3062711	GRCh37/hg19 1p21.2(chr1:100978713-100997065)x1	CDC14A	Copy number loss	not specified	GUncertain significance
Select item 3062700	GRCh37/hg19 1q44(chr1:244579324-246515944)x1	ADSS2, CATSPERE +6 more	Copy number loss	not specified	GPathogenic
Select item 3062689	GRCh37/hg19 1p32.1-31.3(chr1:60641326-65216639)x1	ALG6, ANGPTL3 +16 more	Copy number loss	not specified	GPathogenic
Select item 3062678	GRCh37/hg19 1p36.32(chr1:3575832-4224558)x3	C1orf174, CCDC27 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3062677	GRCh37/hg19 1q43(chr1:239786185-242208644)x1	CHML, CHRM3 +9 more	Copy number loss	not specified	GPathogenic
Select item 3062666	GRCh37/hg19 1q25.3(chr1:183494419-183633454)x1	APOBEC4, ARPC5 +3 more	Copy number loss	not specified	GUncertain significance
Select item 3062655	GRCh37/hg19 1q31.3-32.1(chr1:197216705-203683110)x1	ADIPOR1, ADORA1 +57 more	Copy number loss	not specified	GLikely pathogenic
Select item 3062644	GRCh37/hg19 1q21.1-21.2(chr1:146023922-147831170)x3	ACP6, BCL9 +8 more	Copy number gain	not specified	GPathogenic
Select item 3062633	GRCh37/hg19 1q23.3(chr1:163815650-164647742)x3	PBX1	Copy number gain	not specified	GUncertain significance
Select item 3062622	GRCh37/hg19 1p12(chr1:119666080-119703349)x1	WARS2	Copy number loss	not specified	GUncertain significance
Select item 3062611	GRCh37/hg19 1p22.3(chr1:85513068-86105378)x3	BCL10, C1orf52 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3062600	GRCh37/hg19 1q22(chr1:155902621-156207096)x3	ARHGEF2, KHDC4 +11 more	Copy number gain	not specified	GUncertain significance
Select item 3062587	GRCh37/hg19 1p31.1(chr1:74742161-74907436)x1	FPGT-TNNI3K, TNNI3K	Copy number loss	not specified	GUncertain significance
Select item 3062480	GRCh37/hg19 1q41(chr1:222698623-224065782)x3	AIDA, BROX +11 more	Copy number gain	not specified	GUncertain significance
Select item 3062369	GRCh37/hg19 1q23.3(chr1:161224742-161415981)x3	CFAP126, MPZ +2 more	Copy number gain	not specified	GLikely pathogenic
Select item 3062368	GRCh37/hg19 1q21.2-21.3(chr1:149713775-150385573)x1	ANP32E, APH1A +25 more	Copy number loss	not specified	GPathogenic
Select item 1527725	GRCh37/hg19 1p36.11(chr1:27119557-27547784)	GPATCH3, GPN2 +9 more	Copy number gain	not specified	GUncertain significance
Select item 1527714	GRCh37/hg19 1q44(chr1:246109449-246595110)	SMYD3	Copy number gain	not specified	GUncertain significance
Select item 1527703	GRCh37/hg19 1q43(chr1:241180373-242090901)	CHML, EXO1 +5 more	Copy number gain	not specified	GUncertain significance

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