ClinVar (all) for Orgtrack (Select 319864) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063564	GRCh37/hg19 18p11.32-11.23(chr18:136227-8359829)x1	ADCYAP1, AKAIN1 +28 more	Copy number loss	not specified	GPathogenic
Select item 3063563	GRCh37/hg19 18p11.32-11.21(chr18:136226-14352648)x1	ADCYAP1, AFG3L2 +63 more	Copy number loss	not specified	GPathogenic
Select item 3063562	GRCh37/hg19 18q12.2-21.1(chr18:36823620-44030870)x1	ARK2C, ARK2N +11 more	Copy number loss	not specified	GLikely pathogenic
Select item 3063561	GRCh37/hg19 18q11.1(chr18:18540833-18833060)x3	GREB1L, ROCK1	Copy number gain	not specified	GUncertain significance
Select item 3063560	GRCh37/hg19 18q12.3(chr18:42424349-42622437)x1	SETBP1	Copy number loss	not specified	GPathogenic
Select item 3063559	GRCh37/hg19 18q11.1-12.1(chr18:18529339-26968022)x3	ABHD3, ANKRD29 +29 more	Copy number gain	not specified	GUncertain significance
Select item 3063558	GRCh37/hg19 18p11.32-11.21(chr18:136226-15161581)x1	ADCYAP1, AFG3L2 +65 more	Copy number loss	not specified	GPathogenic
Select item 3063557	GRCh37/hg19 18p11.32-11.31(chr18:544117-5679224)x1	ADCYAP1, AKAIN1 +19 more	Copy number loss	not specified	GPathogenic
Select item 3063556	GRCh37/hg19 18q22.3(chr18:69888150-72001217)x1	C18orf63, CBLN2 +4 more	Copy number loss	not specified	GUncertain significance
Select item 3063555	GRCh37/hg19 18q22.1(chr18:64079710-64330253)x1	CDH19	Copy number loss	not specified	GUncertain significance
Select item 3063554	GRCh37/hg19 2p25.3(chr2:1649820-2022213)x3	MYT1L, PXDN	Copy number gain	not specified	GUncertain significance
Select item 3063553	GRCh37/hg19 18p11.31-11.23(chr18:6737164-7388708)x3	ARHGAP28, LAMA1 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063552	GRCh37/hg19 18q21.2(chr18:52978878-53100587)x1	TCF4	Copy number loss	not specified	GPathogenic
Select item 3063551	GRCh37/hg19 18q22.3-23(chr18:72453821-78014123)x1	ADNP2, ATP9B +19 more	Copy number loss	not specified	GPathogenic
Select item 3063550	GRCh37/hg19 18q22.1-23(chr18:63427506-78014123)x1	ADNP2, ATP9B +37 more	Copy number loss	not specified	GPathogenic
Select item 3063549	GRCh37/hg19 18q11.2(chr18:23648402-24053824)x3	KCTD1, PSMA8 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063548	GRCh37/hg19 18q21.2(chr18:52903599-53084300)x1	TCF4	Copy number loss	not specified	GPathogenic
Select item 3063547	GRCh37/hg19 18q22.3-23(chr18:69968033-78014123)x1	ADNP2, ATP9B +28 more	Copy number loss	not specified	GPathogenic
Select item 3063546	GRCh37/hg19 18q12.1(chr18:28974594-29051649)x3	DSG3, DSG4	Copy number gain	not specified	GUncertain significance
Select item 3063545	GRCh37/hg19 18q12.2-21.1(chr18:33793283-46823898)x1	ARK2C, ARK2N +29 more	Copy number loss	not specified	GPathogenic
Select item 3063544	GRCh37/hg19 18q21.31-23(chr18:55363398-78014123)x1	ADNP2, ALPK2 +72 more	Copy number loss	not specified	GPathogenic
Select item 3063543	GRCh37/hg19 2q11.2(chr2:96917560-96934823)x1	CIAO1, TMEM127	Copy number loss	not specified	GPathogenic
Select item 3063542	GRCh37/hg19 18p11.31-11.21(chr18:2922899-15198990)x3	AFG3L2, AKAIN1 +51 more	Copy number gain	not specified	GPathogenic
Select item 3063541	GRCh37/hg19 18p11.32-11.22(chr18:136226-10365982)x1	ADCYAP1, AKAIN1 +38 more	Copy number loss	not specified	GPathogenic
Select item 3063540	GRCh37/hg19 18p11.32-11.21(chr18:136226-14455323)x3	ADCYAP1, AFG3L2 +63 more	Copy number gain	not specified	GPathogenic
Select item 3063539	GRCh37/hg19 18p11.31-11.23(chr18:6939845-8092116)x3	LAMA1, LRRC30 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063538	GRCh37/hg19 18p11.21(chr18:11200889-12792186)x3	AFG3L2, ANKRD62 +12 more	Copy number gain	not specified	GUncertain significance
Select item 3063537	GRCh37/hg19 18p11.32-11.21(chr18:136226-14148354)x3	ADCYAP1, AFG3L2 +63 more	Copy number gain	not specified	GPathogenic
Select item 3063536	GRCh37/hg19 17q21.33(chr17:48127906-48160869)x1	ITGA3	Copy number loss	not specified	GUncertain significance
Select item 3063535	GRCh37/hg19 17q25.3(chr17:80726070-80841816)x3	TBCD, ZNF750	Copy number gain	not specified	GUncertain significance
Select item 3063534	GRCh37/hg19 17p13.3(chr17:2475401-2725586)x3	CLUH, PAFAH1B1 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063533	GRCh37/hg19 17q25.1(chr17:73281839-73568196)x1	CASKIN2, GRB2 +4 more	Copy number loss	not specified	GUncertain significance
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 3063531	GRCh37/hg19 17q21.33(chr17:48176031-48440167)x3	COL1A1, PDK2 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063530	GRCh37/hg19 17p13.3(chr17:124754-643426)x1	LIAT1, RFLNB +3 more	Copy number loss	not specified	GUncertain significance
Select item 3063529	GRCh37/hg19 17q24.2(chr17:65667922-65892990)x3	BPTF, NOL11 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063528	GRCh37/hg19 17p13.3(chr17:1165433-1225940)x1	BHLHA9, TRARG1	Copy number loss	not specified	GUncertain significance
Select item 3063527	GRCh37/hg19 17p13.3(chr17:1505119-3010963)x1	CLUH, DPH1 +26 more	Copy number loss	not specified	GPathogenic
Select item 3063526	GRCh37/hg19 17p13.3(chr17:2416420-3023516)x3	CLUH, OR1D2 +3 more	Copy number gain	not specified	GUncertain significance
Select item 3063525	GRCh37/hg19 17q23.2(chr17:58950630-59136066)x1	BCAS3	Copy number loss	not specified	GUncertain significance
Select item 3063524	GRCh37/hg19 17p11.2(chr17:16936031-17654594)x3	COPS3, FLCN +7 more	Copy number gain	not specified	GUncertain significance
Select item 3063523	GRCh37/hg19 17p13.3(chr17:1121817-1264198)x3	BHLHA9, TRARG1 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063522	GRCh37/hg19 17q21.31(chr17:41202962-41307101)x1	BRCA1, NBR2	Copy number loss	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 3063520	GRCh37/hg19 17q23.2(chr17:58921973-58999000)x1	BCAS3	Copy number loss	not specified	GUncertain significance
Select item 3063519	GRCh37/hg19 17p11.2(chr17:16096240-16317075)x3	CENPV, NCOR1 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063518	GRCh37/hg19 17p13.3(chr17:1070465-1413071)x1	ABR, BHLHA9 +5 more	Copy number loss	not specified	GPathogenic
Select item 3063517	GRCh37/hg19 17p12-11.2(chr17:15759103-20564268)x1	ADORA2B, AKAP10 +61 more	Copy number loss	not specified	GPathogenic
Select item 3063516	GRCh37/hg19 17p13.3(chr17:1165481-1225940)x1	BHLHA9, TRARG1	Copy number loss	not specified	GUncertain significance
Select item 3063515	GRCh37/hg19 17p13.3(chr17:1483585-1714805)x3	MIR22, PRPF8 +8 more	Copy number gain	not specified	GUncertain significance
Select item 3063514	GRCh37/hg19 17p13.2(chr17:3300933-3536977)x1	ASPA, OR1E1 +6 more	Copy number loss	not specified	GUncertain significance
Select item 3063513	GRCh37/hg19 17q23.2(chr17:60052915-60457049)x3	EFCAB3, MED13	Copy number gain	not specified	GUncertain significance
Select item 3063512	GRCh37/hg19 17p13.3(chr17:2264478-2570762)x3	METTL16, MNT +2 more	Copy number gain	not specified	GLikely pathogenic
Select item 3063511	GRCh37/hg19 17p13.1(chr17:7002380-7469251)x1	PHF23, PLSCR3 +32 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 3063509	GRCh37/hg19 17q11.2(chr17:29305509-31246638)x3	C17orf75, CDK5R1 +16 more	Copy number gain	not specified	GPathogenic
Select item 3063508	GRCh37/hg19 17q12(chr17:35010975-35932571)x3	AATF, ACACA +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063507	GRCh37/hg19 17q25.1(chr17:72875847-73484159)x3	ARMC7, ATP5PD +19 more	Copy number gain	not specified	GUncertain significance
Select item 3063506	GRCh37/hg19 17q21.2(chr17:39705863-40358580)x3	ACLY, CNP +25 more	Copy number gain	not specified	GUncertain significance
Select item 3063505	GRCh37/hg19 17p13.3(chr17:1041646-1305005)x3	ABR, BHLHA9 +2 more	Copy number gain	not specified	GPathogenic
Select item 3063504	GRCh37/hg19 17q21.32(chr17:46867374-46972775)x3	ATP5MC1, CALCOCO2 +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063503	GRCh37/hg19 17p13.2(chr17:5308495-5619495)x3	C1QBP, DERL2 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063502	GRCh37/hg19 17q24.1(chr17:63481404-63618180)x3	AXIN2	Copy number gain	not specified	GUncertain significance
Select item 3063501	GRCh37/hg19 17q11.2(chr17:27281652-27333511)x3	SEZ6	Copy number gain	not specified	GUncertain significance
Select item 3063500	GRCh37/hg19 17p13.3(chr17:1036474-1277162)x3	ABR, BHLHA9 +2 more	Copy number gain	not specified	GLikely pathogenic
Select item 3063499	GRCh37/hg19 1q44(chr1:246179295-246704479)x1	SMYD3, TFB2M	Copy number loss	not specified	GUncertain significance
Select item 3063498	GRCh37/hg19 17q12(chr17:34425362-36371146)x3	AATF, ACACA +23 more	Copy number gain	not specified	GPathogenic
Select item 3063497	GRCh37/hg19 17q25.2(chr17:75077219-75228929)x1	SEC14L1	Copy number loss	not specified	GUncertain significance
Select item 3063496	GRCh37/hg19 17q24.2-24.3(chr17:66271342-67205346)x3	ABCA10, ABCA6 +7 more	Copy number gain	not specified	GUncertain significance
Select item 3063495	GRCh37/hg19 17q12(chr17:33316754-33890206)x1	FNDC8, LIG3 +11 more	Copy number loss	not specified	GUncertain significance
Select item 3063494	GRCh37/hg19 17p13.3-13.2(chr17:2674657-3484368)x3	ASPA, LOC100288728 +14 more	Copy number gain	not specified	GUncertain significance
Select item 3063493	GRCh37/hg19 17p12-11.2(chr17:15872060-16909718)x3	ADORA2B, CCDC144A +11 more	Copy number gain	not specified	GUncertain significance
Select item 3063492	GRCh37/hg19 17p13.3(chr17:2075954-2262703)x3	SGSM2, SMG6 +2 more	Copy number gain	not specified	GUncertain significance
Select item 3063491	GRCh37/hg19 17p13.3(chr17:1165481-1305567)x1	BHLHA9, TRARG1 +1 more	Copy number loss	not specified	GPathogenic
Select item 3063490	GRCh37/hg19 17p11.2(chr17:17065497-17121645)x3	FLCN, MPRIP +1 more	Copy number gain	not specified	GUncertain significance
Select item 3063489	GRCh37/hg19 17p13.3(chr17:1139864-1703566)x3	BHLHA9, CRK +15 more	Copy number gain	not specified	GPathogenic
Select item 3063488	GRCh37/hg19 1q43-44(chr1:243453390-245467768)x1	ADSS2, AKT3 +9 more	Copy number loss	not specified	GPathogenic
Select item 3063487	GRCh37/hg19 17q11.2(chr17:28277040-30903559)x1	ADAP2, ATAD5 +28 more	Copy number loss	not specified	GPathogenic
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 3063485	GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1	ABR, ALOX15 +116 more	Copy number loss	not specified	GPathogenic
Select item 3063484	GRCh37/hg19 17p13.2(chr17:3489513-3557205)x1	CTNS, SHPK +1 more	Copy number loss	not specified	GUncertain significance
Select item 3063483	GRCh37/hg19 17q21.31(chr17:43459741-44292742)x1	ARHGAP27, SPPL2C +5 more	Copy number loss	not specified	GPathogenic
Select item 3063482	GRCh37/hg19 17p13.2(chr17:3489513-3557441)x1	CTNS, SHPK +1 more	Copy number loss	not specified	GPathogenic
Select item 3063481	GRCh37/hg19 17p13.3(chr17:141345-699175)x1	GEMIN4, GLOD4 +6 more	Copy number loss	not specified	GPathogenic
Select item 3063480	GRCh37/hg19 17q23.2(chr17:59909598-59969585)x1	BRIP1, INTS2	Copy number loss	not specified	GPathogenic
Select item 3063479	GRCh37/hg19 17p13.2(chr17:3505568-3557452)x1	CTNS, SHPK +1 more	Copy number loss	not specified	GPathogenic
Select item 3063478	GRCh37/hg19 17p13.2(chr17:3505567-3557452)x1	CTNS, SHPK +1 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 3063476	GRCh37/hg19 17p13.2(chr17:3505567-3557441)x1	CTNS, SHPK +1 more	Copy number loss	not specified	GPathogenic
Select item 3063475	GRCh37/hg19 16q23.3-24.1(chr16:83307393-84530337)x3	ADAD2, ATP2C2 +14 more	Copy number gain	not specified	GUncertain significance
Select item 3063474	GRCh37/hg19 16q23.1(chr16:76339977-76411476)x1	CNTNAP4	Copy number loss	not specified	GUncertain significance
Select item 3063473	GRCh37/hg19 16p13.3(chr16:2130809-2285561)x1	BRICD5, CASKIN1 +8 more	Copy number loss	not specified	GPathogenic
Select item 3063472	GRCh37/hg19 16p13.3(chr16:3598059-3677837)x1	NLRC3, SLX4	Copy number loss	not specified	GUncertain significance
Select item 3063471	GRCh37/hg19 16q24.3(chr16:89462287-89526985)x1	ANKRD11, LOC101927817	Copy number loss	not specified	GPathogenic
Select item 3063470	GRCh37/hg19 16q23.1(chr16:75947360-78217943)x3	ADAMTS18, CLEC3A +6 more	Copy number gain	not specified	GUncertain significance
Select item 3063469	GRCh37/hg19 16p11.2(chr16:28485883-29347116)x1	APOBR, ATP2A1 +15 more	Copy number loss	not specified	GPathogenic
Select item 3063468	GRCh37/hg19 16q24.3(chr16:89692538-89740609)x1	CHMP1A, DPEP1 +1 more	Copy number loss	not specified	GUncertain significance
Select item 3063467	GRCh37/hg19 16q12.2-22.1(chr16:55329260-67180113)x1	ADGRG1, ADGRG3 +85 more	Copy number loss	not specified	GPathogenic
Select item 3063466	GRCh37/hg19 1p12(chr1:119959511-119988221)x1	HSD3B2	Copy number loss	not specified	GUncertain significance
Select item 3063465	GRCh37/hg19 16p13.3(chr16:1252411-1297707)x1	CACNA1H, TPSAB1 +2 more	Copy number loss	not specified	GUncertain significance

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